Canonical Allele Identifier: CA339578452
Gene: FABP3 HGNC NCBI

Linked Data

dbSNP Id: rs1640234723
gnomAD v3: 1-31372981-C-T
gnomAD v4: 1-31372981-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.31372981C>T , CM000663.2:g.31372981C>T GRCh38
NC_000001.10:g.31845828C>T , CM000663.1:g.31845828C>T GRCh37
NC_000001.9:g.31618415C>T NCBI36
NG_047049.1:g.5303G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373713.7:c.34G>A MANE Select ENSP00000362817.2:p.Val12Met
ENST00000373713.6:c.34G>A ENSP00000362817.2:p.Val12Met
ENST00000482018.1:c.34G>A ENSP00000473982.1:p.Val12Met
ENST00000498148.5:c.34G>A ENSP00000474078.1:p.Val12Met
NM_004102.3:c.34G>A NP_004093.1:p.Val12Met
XM_011541007.1:c.34G>A XP_011539309.1:p.Val12Met
NM_001320996.1:c.34G>A NP_001307925.1:p.Val12Met
NM_004102.4:c.34G>A NP_004093.1:p.Val12Met
XM_011541007.3:c.34G>A XP_011539309.1:p.Val12Met
NM_004102.5:c.34G>A MANE Select NP_004093.1:p.Val12Met
NM_001320996.2:c.34G>A NP_001307925.1:p.Val12Met