Canonical Allele Identifier: CA13418924
Gene: FADS2 HGNC NCBI

Linked Data

dbSNP Id: rs174541

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61798436T>C , CM000673.2:g.61798436T>C GRCh38
NC_000011.9:g.61565908T>C , CM000673.1:g.61565908T>C GRCh37
NC_000011.8:g.61322484T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000574708.5:c.-55+5408T>C ENSP00000458917.1:n.-55+5408T>C