Canonical Allele Identifier: CA493797208

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16248772C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154915C>G , CM000678.2:g.16154915C>G	GRCh38
NC_000016.9:g.16248772C>G , CM000678.1:g.16248772C>G	GRCh37
NC_000016.8:g.16156273C>G	NCBI36
NG_007558.2:g.73557G>C
NG_007558.3:g.73703G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000576204.6:n.862G>C
ENST00000622290.5:c.*171G>C	ENSP00000483331.2:n.*171G>C
ENST00000205557.12:c.3999G>C MANE Select	ENSP00000205557.7:p.Val1333=
ENST00000640696.1:c.813G>C	ENSP00000492197.1:p.Val271=
ENST00000205557.11:c.3999G>C	ENSP00000205557.7:p.Val1333=
ENST00000456970.6:c.3624G>C	ENSP00000405002.2:n.3624G>C
ENST00000576204.5:n.862G>C
ENST00000622290.4:c.*1208G>C	ENSP00000483331.1:n.*1208G>C
NM_001171.5:c.3999G>C	NP_001162.4:p.Val1333=
XM_011522479.1:c.3966G>C	XP_011520781.1:p.Val1322=
XM_011522480.1:c.3657G>C	XP_011520782.1:p.Val1219=
XM_011522481.1:c.3657G>C	XP_011520783.1:p.Val1219=
XR_933134.1:n.539-4866C>G
NM_001351800.1:c.3657G>C	NP_001338729.1:p.Val1219=
NR_147784.1:n.3661G>C
XM_011522479.2:c.3966G>C	XP_011520781.1:p.Val1322=
XM_011522481.3:c.3657G>C	XP_011520783.1:p.Val1219=
XM_017023212.1:c.3831G>C	XP_016878701.1:p.Val1277=
XM_024450261.1:c.4035G>C	XP_024306029.1:p.Val1345=
NM_001171.6:c.3999G>C MANE Select	NP_001162.5:p.Val1333=