Canonical Allele Identifier: CA1554387679

Gene: MCCC2

Linked Data

• dbSNP Id: rs1746864399

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71634904T>C , CM000667.2:g.71634904T>C	GRCh38
NC_000005.9:g.70930731T>C , CM000667.1:g.70930731T>C	GRCh37
NC_000005.8:g.70966487T>C	NCBI36
NG_008882.1:g.52617T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000505435.4:n.760-39T>C
ENST00000505787.8:n.2644-39T>C
ENST00000509358.7:c.804-39T>C	ENSP00000420994.3:n.804-39T>C
ENST00000509539.3:c.66-39T>C	ENSP00000425474.3:n.66-39T>C
ENST00000510895.7:n.927-39T>C
ENST00000629193.3:c.690-39T>C	ENSP00000486535.2:n.690-39T>C
ENST00000681968.1:c.297-39T>C	ENSP00000508143.1:n.297-39T>C
ENST00000682045.1:c.660-39T>C	ENSP00000507329.1:n.660-39T>C
ENST00000682214.1:c.411-39T>C	ENSP00000507336.1:n.411-39T>C
ENST00000682499.1:n.1625-39T>C
ENST00000682541.1:c.804-39T>C	ENSP00000507673.1:n.804-39T>C
ENST00000682687.1:c.804-39T>C	ENSP00000507945.1:n.804-39T>C
ENST00000682727.1:c.804-39T>C	ENSP00000507393.1:n.804-39T>C
ENST00000682876.1:c.933-39T>C	ENSP00000508389.1:n.933-39T>C
ENST00000683098.1:c.803+2719T>C	ENSP00000507670.1:n.803+2719T>C
ENST00000683258.1:c.*525-39T>C	ENSP00000507448.1:n.*525-39T>C
ENST00000683339.1:c.588-39T>C	ENSP00000507758.1:n.588-39T>C
ENST00000683403.1:c.804-39T>C	ENSP00000507896.1:n.804-39T>C
ENST00000683429.1:c.411-39T>C	ENSP00000507697.1:n.411-39T>C
ENST00000683665.1:c.804-39T>C	ENSP00000507068.1:n.804-39T>C
ENST00000683789.1:c.690-39T>C	ENSP00000507012.1:n.690-39T>C
ENST00000683847.1:n.648-39T>C
ENST00000683882.1:c.804-39T>C	ENSP00000506735.1:n.804-39T>C
ENST00000684024.1:c.*475-39T>C	ENSP00000507175.1:n.*475-39T>C
ENST00000684254.1:c.*530-39T>C	ENSP00000508001.1:n.*530-39T>C
ENST00000684310.1:c.66-39T>C	ENSP00000507550.1:n.66-39T>C
ENST00000684530.1:c.66-39T>C	ENSP00000507439.1:n.66-39T>C
ENST00000684652.1:n.1767T>C
ENST00000340941.11:c.804-39T>C MANE Select	ENSP00000343657.6:n.804-39T>C
ENST00000340941.10:c.804-39T>C	ENSP00000343657.6:n.804-39T>C
ENST00000505435.3:n.155-39T>C
ENST00000505787.7:n.618-39T>C
ENST00000509358.6:c.804-39T>C	ENSP00000420994.2:n.804-39T>C
ENST00000509539.2:c.129-39T>C	ENSP00000425474.2:n.129-39T>C
ENST00000510895.6:n.418-39T>C
ENST00000512218.6:c.690-39T>C	ENSP00000423202.2:n.690-39T>C
ENST00000629193.2:c.690-39T>C	ENSP00000486535.1:n.690-39T>C
NM_022132.4:c.804-39T>C	NP_071415.1:n.804-39T>C
XM_005248567.1:c.690-39T>C	XP_005248624.1:n.690-39T>C
XM_011543528.1:c.804-39T>C	XP_011541830.1:n.804-39T>C
XM_011543529.1:c.804-39T>C	XP_011541831.1:n.804-39T>C
NM_001363147.1:c.690-39T>C	NP_001350076.1:n.690-39T>C
XM_011543529.2:c.804-39T>C	XP_011541831.1:n.804-39T>C
XM_017009688.1:c.804-39T>C	XP_016865177.1:n.804-39T>C
XR_001742172.1:n.844-39T>C
NM_022132.5:c.804-39T>C MANE Select	NP_071415.1:n.804-39T>C