Canonical Allele Identifier: CA1167208807
Gene: CPT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196749A= , CM000663.2:g.53196749A= GRCh38
NC_000001.10:g.53662421A= , CM000663.1:g.53662421A= GRCh37
NC_000001.9:g.53435009A= NCBI36
NG_008035.1:g.5321A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-195A= ENSP00000360541.3:n.-195A=
NM_000098.2:c.-195A= NP_000089.1:n.-195A=
NM_001330589.1:c.-195A= NP_001317518.1:n.-195A=