Canonical Allele Identifier: CA1083564444
Gene: FABP6 HGNC NCBI

Linked Data

dbSNP Id: rs1760495076

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.160235714G>A , CM000667.2:g.160235714G>A GRCh38
NC_000005.9:g.159662721G>A , CM000667.1:g.159662721G>A GRCh37
NC_000005.8:g.159595299G>A NCBI36
NG_029500.1:g.53348G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000402432.4:c.333+805G>A MANE Select ENSP00000385433.4:n.333+805G>A
ENST00000393980.8:c.480+805G>A ENSP00000377549.4:n.480+805G>A
ENST00000402432.3:c.333+805G>A ENSP00000385433.3:n.333+805G>A
ENST00000521362.1:n.329+805G>A
ENST00000523955.5:c.658+805G>A ENSP00000428766.1:n.658+805G>A
NM_001040442.1:c.480+805G>A NP_001035532.1:n.480+805G>A
NM_001130958.1:c.480+805G>A NP_001124430.1:n.480+805G>A
NM_001445.2:c.333+805G>A NP_001436.1:n.333+805G>A
XM_006714830.2:c.333+805G>A XP_006714893.1:n.333+805G>A
XM_011534463.1:c.396+805G>A XP_011532765.1:n.396+805G>A
NM_001130958.2:c.480+805G>A NP_001124430.1:n.480+805G>A
NM_001445.3:c.333+805G>A MANE Select NP_001436.1:n.333+805G>A