Canonical Allele Identifier: CA416904128

Gene: FABP3

Linked Data

• MyVariant Identifiers: chr1:g.31845793T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.31372946T>G , CM000663.2:g.31372946T>G	GRCh38
NC_000001.10:g.31845793T>G , CM000663.1:g.31845793T>G	GRCh37
NC_000001.9:g.31618380T>G	NCBI36
NG_047049.1:g.5338A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373713.7:c.69A>C MANE Select	ENSP00000362817.2:p.Ser23=
ENST00000373713.6:c.69A>C	ENSP00000362817.2:p.Ser23=
ENST00000482018.1:c.69A>C	ENSP00000473982.1:p.Ser23=
ENST00000498148.5:c.69A>C	ENSP00000474078.1:p.Ser23=
NM_004102.3:c.69A>C	NP_004093.1:p.Ser23=
XM_011541007.1:c.69A>C	XP_011539309.1:p.Ser23=
NM_001320996.1:c.69A>C	NP_001307925.1:p.Ser23=
NM_004102.4:c.69A>C	NP_004093.1:p.Ser23=
XM_011541007.3:c.69A>C	XP_011539309.1:p.Ser23=
NM_004102.5:c.69A>C MANE Select	NP_004093.1:p.Ser23=
NM_001320996.2:c.69A>C	NP_001307925.1:p.Ser23=