Canonical Allele Identifier: CA147076750

Gene: FABP7

Linked Data

• dbSNP Id: rs918424273
• gnomAD v2: 6-123101381-T-G
• gnomAD v3: 6-122780236-T-G
• gnomAD v4: 6-122780236-T-G
• MyVariant Identifiers: chr6:g.123101381T>G (hg19) ; chr6:g.122780236T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.122780236T>G , CM000668.2:g.122780236T>G	GRCh38
NC_000006.11:g.123101381T>G , CM000668.1:g.123101381T>G	GRCh37
NC_000006.10:g.123143080T>G	NCBI36
NG_050619.1:g.36036T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000368444.8:c.74-55T>G MANE Select	ENSP00000357429.3:n.74-55T>G
ENST00000356535.4:c.74-55T>G	ENSP00000348931.4:n.74-55T>G
ENST00000368444.7:c.74-55T>G	ENSP00000357429.3:n.74-55T>G
NM_001446.3:c.74-55T>G	NP_001437.1:n.74-55T>G
XM_005266858.2:c.74-55T>G	XP_005266915.1:n.74-55T>G
NM_001319039.1:c.74-55T>G	NP_001305968.1:n.74-55T>G
NM_001319041.1:c.74-55T>G	NP_001305970.1:n.74-55T>G
NM_001319042.1:c.62-55T>G	NP_001305971.1:n.62-55T>G
NM_001446.4:c.74-55T>G	NP_001437.1:n.74-55T>G
NM_001446.5:c.74-55T>G MANE Select	NP_001437.1:n.74-55T>G
NM_001319041.2:c.74-55T>G	NP_001305970.1:n.74-55T>G
NM_001319039.2:c.74-55T>G	NP_001305968.1:n.74-55T>G
NM_001319042.2:c.62-55T>G	NP_001305971.1:n.62-55T>G