Canonical Allele Identifier: CA20151292

Gene: FABP3

Linked Data

• dbSNP Id: rs200552069
• gnomAD v2: 1-31845903-G-A
• gnomAD v3: 1-31373056-G-A
• gnomAD v4: 1-31373056-G-A
• MyVariant Identifiers: chr1:g.31845903G>A (hg19) ; chr1:g.31373056G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.31373056G>A , CM000663.2:g.31373056G>A	GRCh38
NC_000001.10:g.31845903G>A , CM000663.1:g.31845903G>A	GRCh37
NC_000001.9:g.31618490G>A	NCBI36
NG_047049.1:g.5228C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373713.7:c.-42C>T MANE Select	ENSP00000362817.2:n.-42C>T
ENST00000373713.6:c.-42C>T	ENSP00000362817.2:n.-42C>T
ENST00000482018.1:c.-27-15C>T	ENSP00000473982.1:n.-27-15C>T
ENST00000498148.5:c.-42C>T	ENSP00000474078.1:n.-42C>T
NM_004102.3:c.-42C>T	NP_004093.1:n.-42C>T
XM_011541007.1:c.-42C>T	XP_011539309.1:n.-42C>T
NM_001320996.1:c.-42C>T	NP_001307925.1:n.-42C>T
NM_004102.4:c.-42C>T	NP_004093.1:n.-42C>T
XM_011541007.3:c.-42C>T	XP_011539309.1:n.-42C>T
NM_004102.5:c.-42C>T MANE Select	NP_004093.1:n.-42C>T
NM_001320996.2:c.-42C>T	NP_001307925.1:n.-42C>T