Canonical Allele Identifier: CA1167208831
Gene: CPT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196774G= , CM000663.2:g.53196774G= GRCh38
NC_000001.10:g.53662446G= , CM000663.1:g.53662446G= GRCh37
NC_000001.9:g.53435034G= NCBI36
NG_008035.1:g.5346G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-170G= ENSP00000360541.3:n.-170G=
NM_000098.2:c.-170G= NP_000089.1:n.-170G=
XM_005270484.1:c.-170G= XP_005270541.1:n.-170G=
NM_001330589.1:c.-170G= NP_001317518.1:n.-170G=