Canonical Allele Identifier: CA2052273159
Gene: MGAT4C HGNC NCBI

Linked Data

dbSNP Id: rs1951229120
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.86751353G>T , CM000674.2:g.86751353G>T GRCh38
NC_000012.11:g.87145130G>T , CM000674.1:g.87145130G>T GRCh37
NC_000012.10:g.85669261G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000548651.6:c.-261-24112C>A ENSP00000447253.1:n.-261-24112C>A
ENST00000621808.5:c.-381-24112C>A ENSP00000478300.1:n.-381-24112C>A
ENST00000551921.2:n.240-24112C>A
ENST00000621808.4:c.-381-24112C>A ENSP00000478300.1:n.-381-24112C>A
NM_013244.3:c.-229+87313C>A NP_037376.2:n.-229+87313C>A
NM_001351285.1:c.-326-24112C>A NP_001338214.1:n.-326-24112C>A
NM_001351286.1:c.-261-24112C>A NP_001338215.1:n.-261-24112C>A
NM_013244.4:c.-229+87313C>A NP_037376.2:n.-229+87313C>A
NM_001351285.2:c.-326-24112C>A NP_001338214.1:n.-326-24112C>A
NM_001351286.2:c.-261-24112C>A NP_001338215.1:n.-261-24112C>A
NM_013244.5:c.-229+87313C>A NP_037376.2:n.-229+87313C>A
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