Canonical Allele Identifier: CA451977612

Gene: FABP7

Linked Data

• MyVariant Identifiers: chr6:g.123101557C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.122780412C>T , CM000668.2:g.122780412C>T	GRCh38
NC_000006.11:g.123101557C>T , CM000668.1:g.123101557C>T	GRCh37
NC_000006.10:g.123143256C>T	NCBI36
NG_050619.1:g.36212C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000368444.8:c.195C>T MANE Select	ENSP00000357429.3:p.Phe65=
ENST00000356535.4:c.195C>T	ENSP00000348931.4:p.Phe65=
ENST00000368444.7:c.195C>T	ENSP00000357429.3:p.Phe65=
NM_001446.3:c.195C>T	NP_001437.1:p.Phe65=
XM_005266858.2:c.195C>T	XP_005266915.1:p.Phe65=
NM_001319039.1:c.195C>T	NP_001305968.1:p.Phe65=
NM_001319041.1:c.195C>T	NP_001305970.1:p.Phe65=
NM_001319042.1:c.183C>T	NP_001305971.1:p.Phe61=
NM_001446.4:c.195C>T	NP_001437.1:p.Phe65=
NM_001446.5:c.195C>T MANE Select	NP_001437.1:p.Phe65=
NM_001319041.2:c.195C>T	NP_001305970.1:p.Phe65=
NM_001319039.2:c.195C>T	NP_001305968.1:p.Phe65=
NM_001319042.2:c.183C>T	NP_001305971.1:p.Phe61=