Canonical Allele Identifier: CA607285641

Gene: MMAB

Linked Data

• dbSNP Id: rs1215310154
• gnomAD v2: 12-109999028-C-T
• gnomAD v4: 12-109561223-C-T
• MyVariant Identifiers: chr12:g.109999028C>T (hg19) ; chr12:g.109561223C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109561223C>T , CM000674.2:g.109561223C>T	GRCh38
NC_000012.11:g.109999028C>T , CM000674.1:g.109999028C>T	GRCh37
NC_000012.10:g.108483411C>T	NCBI36
NG_007096.1:g.17275G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.520-119G>A MANE Select	ENSP00000445920.1:n.520-119G>A
ENST00000537496.5:c.*84+20G>A	ENSP00000444793.1:n.*84+20G>A
ENST00000540016.5:c.364-119G>A	ENSP00000474582.1:n.364-119G>A
ENST00000541763.6:c.626G>A	ENSP00000474981.1:n.626G>A
ENST00000544051.5:c.*400+20G>A	ENSP00000438079.1:n.*400+20G>A
ENST00000545712.6:c.520-119G>A	ENSP00000445920.1:n.520-119G>A
NM_052845.3:c.520-119G>A	NP_443077.1:n.520-119G>A
NR_038118.1:n.679+20G>A
XM_011538266.1:c.364+20G>A	XP_011536568.1:n.364+20G>A
XM_011538267.1:c.364+20G>A	XP_011536569.1:n.364+20G>A
XM_011538268.1:c.247-119G>A	XP_011536570.1:n.247-119G>A
XM_011538269.1:c.244-119G>A	XP_011536571.1:n.244-119G>A
XM_011538267.3:c.364+20G>A	XP_011536569.1:n.364+20G>A
XM_011538268.2:c.247-119G>A	XP_011536570.1:n.247-119G>A
XM_011538269.2:c.244-119G>A	XP_011536571.1:n.244-119G>A
XM_024448961.1:c.520-119G>A	XP_024304729.1:n.520-119G>A
NM_052845.4:c.520-119G>A MANE Select	NP_443077.1:n.520-119G>A
NR_038118.2:n.630+20G>A