Canonical Allele Identifier: CA243447503

Gene: MMAB

Linked Data

• dbSNP Id: rs577697260
• gnomAD v2: 12-109995044-C-T
• gnomAD v3: 12-109557239-C-T
• gnomAD v4: 12-109557239-C-T
• MyVariant Identifiers: chr12:g.109995044C>T (hg19) ; chr12:g.109557239C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109557239C>T , CM000674.2:g.109557239C>T	GRCh38
NC_000012.11:g.109995044C>T , CM000674.1:g.109995044C>T	GRCh37
NC_000012.10:g.108479427C>T	NCBI36
NG_007096.1:g.21259G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.645-103G>A MANE Select	ENSP00000445920.1:n.645-103G>A
ENST00000537496.5:c.*210-103G>A	ENSP00000444793.1:n.*210-103G>A
ENST00000540016.5:c.489-103G>A	ENSP00000474582.1:n.489-103G>A
ENST00000541763.6:c.870-103G>A	ENSP00000474981.1:n.870-103G>A
ENST00000544051.5:c.*526-103G>A	ENSP00000438079.1:n.*526-103G>A
ENST00000545712.6:c.645-103G>A	ENSP00000445920.1:n.645-103G>A
NM_052845.3:c.645-103G>A	NP_443077.1:n.645-103G>A
NR_038118.1:n.805-103G>A
XM_011538266.1:c.490-103G>A	XP_011536568.1:n.490-103G>A
XM_011538267.1:c.490-103G>A	XP_011536569.1:n.490-103G>A
XM_011538268.1:c.372-103G>A	XP_011536570.1:n.372-103G>A
XM_011538269.1:c.369-103G>A	XP_011536571.1:n.369-103G>A
XM_011538267.3:c.490-103G>A	XP_011536569.1:n.490-103G>A
XM_011538268.2:c.372-103G>A	XP_011536570.1:n.372-103G>A
XM_011538269.2:c.369-103G>A	XP_011536571.1:n.369-103G>A
NM_052845.4:c.645-103G>A MANE Select	NP_443077.1:n.645-103G>A
NR_038118.2:n.756-103G>A