Canonical Allele Identifier: CA481712497

Gene: MMAB

Linked Data

• ClinVar Variation Id: 2025042
• ClinVar RCV Id: RCV002848144
• MyVariant Identifiers: chr12:g.110006646T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109568841T>C , CM000674.2:g.109568841T>C	GRCh38
NC_000012.11:g.110006646T>C , CM000674.1:g.110006646T>C	GRCh37
NC_000012.10:g.108491029T>C	NCBI36
NG_007096.1:g.9657A>G
NG_007702.1:g.147T>C , LRG_156:g.147T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545712.7:c.219A>G MANE Select	ENSP00000445920.1:p.Gly73=
ENST00000420167.6:c.*48A>G	ENSP00000416136.2:n.*48A>G
ENST00000503497.7:c.219A>G	ENSP00000474881.1:p.Gly73=
ENST00000536760.1:n.222A>G
ENST00000537236.2:c.219A>G	ENSP00000483818.1:p.Gly73=
ENST00000537496.5:c.219A>G	ENSP00000444793.1:p.Gly73=
ENST00000540016.5:c.135-3665A>G	ENSP00000474582.1:n.135-3665A>G
ENST00000541763.6:c.219A>G	ENSP00000474981.1:p.Gly73=
ENST00000542390.5:n.246A>G
ENST00000544051.5:c.*13A>G	ENSP00000438079.1:n.*13A>G
ENST00000545712.6:c.219A>G	ENSP00000445920.1:p.Gly73=
NM_052845.3:c.219A>G	NP_443077.1:p.Gly73=
NR_038118.1:n.292A>G
XM_024448961.1:c.219A>G	XP_024304729.1:p.Gly73=
NM_052845.4:c.219A>G MANE Select	NP_443077.1:p.Gly73=
NR_038118.2:n.243A>G