Canonical Allele Identifier: CA2680210746
Gene: FABP7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.122780213G>T , CM000668.2:g.122780213G>T GRCh38
NC_000006.11:g.123101358G>T , CM000668.1:g.123101358G>T GRCh37
NC_000006.10:g.123143057G>T NCBI36
NG_050619.1:g.36013G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000368444.8:c.74-78G>T MANE Select ENSP00000357429.3:n.74-78G>T
ENST00000356535.4:c.74-78G>T ENSP00000348931.4:n.74-78G>T
ENST00000368444.7:c.74-78G>T ENSP00000357429.3:n.74-78G>T
NM_001446.3:c.74-78G>T NP_001437.1:n.74-78G>T
XM_005266858.2:c.74-78G>T XP_005266915.1:n.74-78G>T
NM_001319039.1:c.74-78G>T NP_001305968.1:n.74-78G>T
NM_001319041.1:c.74-78G>T NP_001305970.1:n.74-78G>T
NM_001319042.1:c.62-78G>T NP_001305971.1:n.62-78G>T
NM_001446.4:c.74-78G>T NP_001437.1:n.74-78G>T
NM_001446.5:c.74-78G>T MANE Select NP_001437.1:n.74-78G>T
NM_001319041.2:c.74-78G>T NP_001305970.1:n.74-78G>T
NM_001319039.2:c.74-78G>T NP_001305968.1:n.74-78G>T
NM_001319042.2:c.62-78G>T NP_001305971.1:n.62-78G>T