Canonical Allele Identifier: CA451977557

Gene: FABP7

Linked Data

• MyVariant Identifiers: chr6:g.123101464A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.122780319A>C , CM000668.2:g.122780319A>C	GRCh38
NC_000006.11:g.123101464A>C , CM000668.1:g.123101464A>C	GRCh37
NC_000006.10:g.123143163A>C	NCBI36
NG_050619.1:g.36119A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368444.8:c.102A>C MANE Select	ENSP00000357429.3:p.Gly34=
ENST00000356535.4:c.102A>C	ENSP00000348931.4:p.Gly34=
ENST00000368444.7:c.102A>C	ENSP00000357429.3:p.Gly34=
NM_001446.3:c.102A>C	NP_001437.1:p.Gly34=
XM_005266858.2:c.102A>C	XP_005266915.1:p.Gly34=
NM_001319039.1:c.102A>C	NP_001305968.1:p.Gly34=
NM_001319041.1:c.102A>C	NP_001305970.1:p.Gly34=
NM_001319042.1:c.90A>C	NP_001305971.1:p.Gly30=
NM_001446.4:c.102A>C	NP_001437.1:p.Gly34=
NM_001446.5:c.102A>C MANE Select	NP_001437.1:p.Gly34=
NM_001319041.2:c.102A>C	NP_001305970.1:p.Gly34=
NM_001319039.2:c.102A>C	NP_001305968.1:p.Gly34=
NM_001319042.2:c.90A>C	NP_001305971.1:p.Gly30=