Canonical Allele Identifier: CA1000199692
Gene: FABP3 HGNC NCBI

Linked Data

dbSNP Id: rs1569983365
gnomAD v3: 1-31373138-C-T
gnomAD v4: 1-31373138-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.31373138C>T , CM000663.2:g.31373138C>T GRCh38
NC_000001.10:g.31845985C>T , CM000663.1:g.31845985C>T GRCh37
NC_000001.9:g.31618572C>T NCBI36
NG_047049.1:g.5146G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000482018.1:c.-27-97G>A ENSP00000473982.1:n.-27-97G>A
XM_011541007.1:c.-124G>A XP_011539309.1:n.-124G>A
NM_001320996.1:c.-124G>A NP_001307925.1:n.-124G>A
NM_004102.4:c.-124G>A NP_004093.1:n.-124G>A
XM_011541007.3:c.-124G>A XP_011539309.1:n.-124G>A