Canonical Allele Identifier: CA451977608

Gene: FABP7

Linked Data

• MyVariant Identifiers: chr6:g.123101548G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.122780403G>A , CM000668.2:g.122780403G>A	GRCh38
NC_000006.11:g.123101548G>A , CM000668.1:g.123101548G>A	GRCh37
NC_000006.10:g.123143247G>A	NCBI36
NG_050619.1:g.36203G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368444.8:c.186G>A MANE Select	ENSP00000357429.3:p.Glu62=
ENST00000356535.4:c.186G>A	ENSP00000348931.4:p.Glu62=
ENST00000368444.7:c.186G>A	ENSP00000357429.3:p.Glu62=
NM_001446.3:c.186G>A	NP_001437.1:p.Glu62=
XM_005266858.2:c.186G>A	XP_005266915.1:p.Glu62=
NM_001319039.1:c.186G>A	NP_001305968.1:p.Glu62=
NM_001319041.1:c.186G>A	NP_001305970.1:p.Glu62=
NM_001319042.1:c.174G>A	NP_001305971.1:p.Glu58=
NM_001446.4:c.186G>A	NP_001437.1:p.Glu62=
NM_001446.5:c.186G>A MANE Select	NP_001437.1:p.Glu62=
NM_001319041.2:c.186G>A	NP_001305970.1:p.Glu62=
NM_001319039.2:c.186G>A	NP_001305968.1:p.Glu62=
NM_001319042.2:c.174G>A	NP_001305971.1:p.Glu58=