Canonical Allele Identifier: CA136908843
Gene: AGPAT1 HGNC NCBI

Linked Data

dbSNP Id: rs990429006
MyVariant Identifiers: chr6:g.32145677T>C (hg19) chr6:g.32177900T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32177900T>C , CM000668.2:g.32177900T>C GRCh38
NC_000006.11:g.32145677T>C , CM000668.1:g.32145677T>C GRCh37
NC_000006.10:g.32253655T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000336984.6:c.-10+101A>G ENSP00000337463.6:n.-10+101A>G
NM_032741.4:c.-10+101A>G NP_116130.2:n.-10+101A>G
NM_032741.5:c.-10+101A>G NP_116130.2:n.-10+101A>G
Search 100 bp 5'
Search 100 bp 3'