Canonical Allele Identifier: CA365489016

Gene: FABP7

Linked Data

• dbSNP Id: rs1379572386
• gnomAD v2: 6-123101547-A-T
• MyVariant Identifiers: chr6:g.123101547A>T (hg19) ; chr6:g.122780402A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.122780402A>T , CM000668.2:g.122780402A>T	GRCh38
NC_000006.11:g.123101547A>T , CM000668.1:g.123101547A>T	GRCh37
NC_000006.10:g.123143246A>T	NCBI36
NG_050619.1:g.36202A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000368444.8:c.185A>T MANE Select	ENSP00000357429.3:p.Glu62Val
ENST00000356535.4:c.185A>T	ENSP00000348931.4:p.Glu62Val
ENST00000368444.7:c.185A>T	ENSP00000357429.3:p.Glu62Val
NM_001446.3:c.185A>T	NP_001437.1:p.Glu62Val
XM_005266858.2:c.185A>T	XP_005266915.1:p.Glu62Val
NM_001319039.1:c.185A>T	NP_001305968.1:p.Glu62Val
NM_001319041.1:c.185A>T	NP_001305970.1:p.Glu62Val
NM_001319042.1:c.173A>T	NP_001305971.1:p.Glu58Val
NM_001446.4:c.185A>T	NP_001437.1:p.Glu62Val
NM_001446.5:c.185A>T MANE Select	NP_001437.1:p.Glu62Val
NM_001319041.2:c.185A>T	NP_001305970.1:p.Glu62Val
NM_001319039.2:c.185A>T	NP_001305968.1:p.Glu62Val
NM_001319042.2:c.173A>T	NP_001305971.1:p.Glu58Val