Canonical Allele Identifier: CA2620809895

Gene: MMAB

Linked Data

• gnomAD v4: 12-109556919-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109556919T>C , CM000674.2:g.109556919T>C	GRCh38
NC_000012.11:g.109994724T>C , CM000674.1:g.109994724T>C	GRCh37
NC_000012.10:g.108479107T>C	NCBI36
NG_007096.1:g.21579A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.*109A>G MANE Select	ENSP00000445920.1:n.*109A>G
ENST00000537496.5:c.*427A>G	ENSP00000444793.1:n.*427A>G
ENST00000540016.5:c.*109A>G	ENSP00000474582.1:n.*109A>G
ENST00000541763.6:c.1087A>G	ENSP00000474981.1:n.1087A>G
ENST00000544051.5:c.*743A>G	ENSP00000438079.1:n.*743A>G
ENST00000545712.6:c.*109A>G	ENSP00000445920.1:n.*109A>G
NM_052845.3:c.*109A>G	NP_443077.1:n.*109A>G
NR_038118.1:n.1022A>G
XM_011538266.1:c.*209A>G	XP_011536568.1:n.*209A>G
XM_011538267.1:c.*209A>G	XP_011536569.1:n.*209A>G
XM_011538268.1:c.*109A>G	XP_011536570.1:n.*109A>G
XM_011538269.1:c.*109A>G	XP_011536571.1:n.*109A>G
XM_011538267.3:c.*209A>G	XP_011536569.1:n.*209A>G
XM_011538268.2:c.*109A>G	XP_011536570.1:n.*109A>G
XM_011538269.2:c.*109A>G	XP_011536571.1:n.*109A>G
NM_052845.4:c.*109A>G MANE Select	NP_443077.1:n.*109A>G
NR_038118.2:n.973A>G