Canonical Allele Identifier: CA365489032

Gene: FABP7

Linked Data

• MyVariant Identifiers: chr6:g.123101554T>G (hg19) ; chr6:g.122780409T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.122780409T>G , CM000668.2:g.122780409T>G	GRCh38
NC_000006.11:g.123101554T>G , CM000668.1:g.123101554T>G	GRCh37
NC_000006.10:g.123143253T>G	NCBI36
NG_050619.1:g.36209T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000368444.8:c.192T>G MANE Select	ENSP00000357429.3:p.Ser64Arg
ENST00000356535.4:c.192T>G	ENSP00000348931.4:p.Ser64Arg
ENST00000368444.7:c.192T>G	ENSP00000357429.3:p.Ser64Arg
NM_001446.3:c.192T>G	NP_001437.1:p.Ser64Arg
XM_005266858.2:c.192T>G	XP_005266915.1:p.Ser64Arg
NM_001319039.1:c.192T>G	NP_001305968.1:p.Ser64Arg
NM_001319041.1:c.192T>G	NP_001305970.1:p.Ser64Arg
NM_001319042.1:c.180T>G	NP_001305971.1:p.Ser60Arg
NM_001446.4:c.192T>G	NP_001437.1:p.Ser64Arg
NM_001446.5:c.192T>G MANE Select	NP_001437.1:p.Ser64Arg
NM_001319041.2:c.192T>G	NP_001305970.1:p.Ser64Arg
NM_001319039.2:c.192T>G	NP_001305968.1:p.Ser64Arg
NM_001319042.2:c.180T>G	NP_001305971.1:p.Ser60Arg