Canonical Allele Identifier: CA806484938

Gene: FABP6

Linked Data

• dbSNP Id: rs1469235765
• gnomAD v3: 5-160235685-T-G
• gnomAD v4: 5-160235685-T-G
• MyVariant Identifiers: chr5:g.159662692T>G (hg19) ; chr5:g.160235685T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.160235685T>G , CM000667.2:g.160235685T>G	GRCh38
NC_000005.9:g.159662692T>G , CM000667.1:g.159662692T>G	GRCh37
NC_000005.8:g.159595270T>G	NCBI36
NG_029500.1:g.53319T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000402432.4:c.333+776T>G MANE Select	ENSP00000385433.4:n.333+776T>G
ENST00000393980.8:c.480+776T>G	ENSP00000377549.4:n.480+776T>G
ENST00000402432.3:c.333+776T>G	ENSP00000385433.3:n.333+776T>G
ENST00000521362.1:n.329+776T>G
ENST00000523955.5:c.658+776T>G	ENSP00000428766.1:n.658+776T>G
NM_001040442.1:c.480+776T>G	NP_001035532.1:n.480+776T>G
NM_001130958.1:c.480+776T>G	NP_001124430.1:n.480+776T>G
NM_001445.2:c.333+776T>G	NP_001436.1:n.333+776T>G
XM_006714830.2:c.333+776T>G	XP_006714893.1:n.333+776T>G
XM_011534463.1:c.396+776T>G	XP_011532765.1:n.396+776T>G
NM_001130958.2:c.480+776T>G	NP_001124430.1:n.480+776T>G
NM_001445.3:c.333+776T>G MANE Select	NP_001436.1:n.333+776T>G