Canonical Allele Identifier: CA3982901
Gene: FABP7 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2279381

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.122780399C>T , CM000668.2:g.122780399C>T GRCh38
NC_000006.10:g.123143243C>T NCBI36
NC_000006.11:g.123101544C>T , CM000668.1:g.123101544C>T GRCh37
NG_050619.1:g.36199C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000356535.4:c.182C>T ENSP00000348931.4:p.Thr61Met
ENST00000368444.7:c.182C>T ENSP00000357429.3:p.Thr61Met
NM_001446.3:c.182C>T VV NP_001437.1:p.Thr61Met
XM_005266858.2:c.182C>T XP_005266915.1:p.Thr61Met
NM_001319039.1:c.182C>T VV NP_001305968.1:p.Thr61Met
NM_001319041.1:c.182C>T VV NP_001305970.1:p.Thr61Met
NM_001319042.1:c.170C>T VV NP_001305971.1:p.Thr57Met
NM_001446.4:c.182C>T VV