Canonical Allele Identifier: CA2600517645

Gene: MGAT4C

Linked Data

• dbSNP Id: rs1951229669
• gnomAD v3: 12-86751392-T-C
• gnomAD v4: 12-86751392-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.86751392T>C , CM000674.2:g.86751392T>C	GRCh38
NC_000012.11:g.87145169T>C , CM000674.1:g.87145169T>C	GRCh37
NC_000012.10:g.85669300T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000548651.6:c.-261-24151A>G	ENSP00000447253.1:n.-261-24151A>G
ENST00000621808.5:c.-381-24151A>G	ENSP00000478300.1:n.-381-24151A>G
ENST00000551921.2:n.240-24151A>G
ENST00000621808.4:c.-381-24151A>G	ENSP00000478300.1:n.-381-24151A>G
NM_013244.3:c.-229+87274A>G	NP_037376.2:n.-229+87274A>G
NM_001351285.1:c.-326-24151A>G	NP_001338214.1:n.-326-24151A>G
NM_001351286.1:c.-261-24151A>G	NP_001338215.1:n.-261-24151A>G
NM_013244.4:c.-229+87274A>G	NP_037376.2:n.-229+87274A>G
NM_001351285.2:c.-326-24151A>G	NP_001338214.1:n.-326-24151A>G
NM_001351286.2:c.-261-24151A>G	NP_001338215.1:n.-261-24151A>G
NM_013244.5:c.-229+87274A>G	NP_037376.2:n.-229+87274A>G