Canonical Allele Identifier: CA730597

Gene: FABP3

Linked Data

• dbSNP Id: rs183662956
• ExAC: 1:31845892 C / G
• gnomAD v2: 1-31845892-C-G
• gnomAD v3: 1-31373045-C-G
• gnomAD v4: 1-31373045-C-G
• MyVariant Identifiers: chr1:g.31845892C>G (hg19) ; chr1:g.31373045C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.31373045C>G , CM000663.2:g.31373045C>G	GRCh38
NC_000001.10:g.31845892C>G , CM000663.1:g.31845892C>G	GRCh37
NC_000001.9:g.31618479C>G	NCBI36
NG_047049.1:g.5239G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373713.7:c.-31G>C MANE Select	ENSP00000362817.2:n.-31G>C
ENST00000373713.6:c.-31G>C	ENSP00000362817.2:n.-31G>C
ENST00000482018.1:c.-27-4G>C	ENSP00000473982.1:n.-27-4G>C
ENST00000498148.5:c.-31G>C	ENSP00000474078.1:n.-31G>C
NM_004102.3:c.-31G>C	NP_004093.1:n.-31G>C
XM_011541007.1:c.-31G>C	XP_011539309.1:n.-31G>C
NM_001320996.1:c.-31G>C	NP_001307925.1:n.-31G>C
NM_004102.4:c.-31G>C	NP_004093.1:n.-31G>C
XM_011541007.3:c.-31G>C	XP_011539309.1:n.-31G>C
NM_004102.5:c.-31G>C MANE Select	NP_004093.1:n.-31G>C
NM_001320996.2:c.-31G>C	NP_001307925.1:n.-31G>C