Canonical Allele Identifier: CA481710156

Gene: MMAB

Linked Data

• MyVariant Identifiers: chr12:g.109994929A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109557124A>G , CM000674.2:g.109557124A>G	GRCh38
NC_000012.11:g.109994929A>G , CM000674.1:g.109994929A>G	GRCh37
NC_000012.10:g.108479312A>G	NCBI36
NG_007096.1:g.21374T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.657T>C MANE Select	ENSP00000445920.1:p.Tyr219=
ENST00000537496.5:c.*222T>C	ENSP00000444793.1:n.*222T>C
ENST00000540016.5:c.501T>C	ENSP00000474582.1:p.Tyr167=
ENST00000541763.6:c.882T>C	ENSP00000474981.1:n.882T>C
ENST00000544051.5:c.*538T>C	ENSP00000438079.1:n.*538T>C
ENST00000545712.6:c.657T>C	ENSP00000445920.1:p.Tyr219=
NM_052845.3:c.657T>C	NP_443077.1:p.Tyr219=
NR_038118.1:n.817T>C
XM_011538266.1:c.*4T>C	XP_011536568.1:n.*4T>C
XM_011538267.1:c.*4T>C	XP_011536569.1:n.*4T>C
XM_011538268.1:c.384T>C	XP_011536570.1:p.Tyr128=
XM_011538269.1:c.381T>C	XP_011536571.1:p.Tyr127=
XM_011538267.3:c.*4T>C	XP_011536569.1:n.*4T>C
XM_011538268.2:c.384T>C	XP_011536570.1:p.Tyr128=
XM_011538269.2:c.381T>C	XP_011536571.1:p.Tyr127=
NM_052845.4:c.657T>C MANE Select	NP_443077.1:p.Tyr219=
NR_038118.2:n.768T>C