Canonical Allele Identifier: CA692989719

Gene: MGAT4C

Linked Data

• dbSNP Id: rs1226315985
• gnomAD v3: 12-86751326-T-G
• gnomAD v4: 12-86751326-T-G
• MyVariant Identifiers: chr12:g.87145103T>G (hg19) ; chr12:g.86751326T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.86751326T>G , CM000674.2:g.86751326T>G	GRCh38
NC_000012.11:g.87145103T>G , CM000674.1:g.87145103T>G	GRCh37
NC_000012.10:g.85669234T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000548651.6:c.-261-24085A>C	ENSP00000447253.1:n.-261-24085A>C
ENST00000621808.5:c.-381-24085A>C	ENSP00000478300.1:n.-381-24085A>C
ENST00000551921.2:n.240-24085A>C
ENST00000621808.4:c.-381-24085A>C	ENSP00000478300.1:n.-381-24085A>C
NM_013244.3:c.-229+87340A>C	NP_037376.2:n.-229+87340A>C
NM_001351285.1:c.-326-24085A>C	NP_001338214.1:n.-326-24085A>C
NM_001351286.1:c.-261-24085A>C	NP_001338215.1:n.-261-24085A>C
NM_013244.4:c.-229+87340A>C	NP_037376.2:n.-229+87340A>C
NM_001351285.2:c.-326-24085A>C	NP_001338214.1:n.-326-24085A>C
NM_001351286.2:c.-261-24085A>C	NP_001338215.1:n.-261-24085A>C
NM_013244.5:c.-229+87340A>C	NP_037376.2:n.-229+87340A>C