Canonical Allele Identifier: CA2620810731

Gene: MMAB

Linked Data

• gnomAD v4: 12-109561217-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109561217C>G , CM000674.2:g.109561217C>G	GRCh38
NC_000012.11:g.109999022C>G , CM000674.1:g.109999022C>G	GRCh37
NC_000012.10:g.108483405C>G	NCBI36
NG_007096.1:g.17281G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.520-113G>C MANE Select	ENSP00000445920.1:n.520-113G>C
ENST00000537496.5:c.*84+26G>C	ENSP00000444793.1:n.*84+26G>C
ENST00000540016.5:c.364-113G>C	ENSP00000474582.1:n.364-113G>C
ENST00000541763.6:c.632G>C	ENSP00000474981.1:n.632G>C
ENST00000544051.5:c.*400+26G>C	ENSP00000438079.1:n.*400+26G>C
ENST00000545712.6:c.520-113G>C	ENSP00000445920.1:n.520-113G>C
NM_052845.3:c.520-113G>C	NP_443077.1:n.520-113G>C
NR_038118.1:n.679+26G>C
XM_011538266.1:c.364+26G>C	XP_011536568.1:n.364+26G>C
XM_011538267.1:c.364+26G>C	XP_011536569.1:n.364+26G>C
XM_011538268.1:c.247-113G>C	XP_011536570.1:n.247-113G>C
XM_011538269.1:c.244-113G>C	XP_011536571.1:n.244-113G>C
XM_011538267.3:c.364+26G>C	XP_011536569.1:n.364+26G>C
XM_011538268.2:c.247-113G>C	XP_011536570.1:n.247-113G>C
XM_011538269.2:c.244-113G>C	XP_011536571.1:n.244-113G>C
XM_024448961.1:c.520-113G>C	XP_024304729.1:n.520-113G>C
NM_052845.4:c.520-113G>C MANE Select	NP_443077.1:n.520-113G>C
NR_038118.2:n.630+26G>C