Canonical Allele Identifier: CA1167208771
Gene: CPT2 HGNC NCBI

Linked Data

dbSNP Id: rs1572377984

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196699C>A , CM000663.2:g.53196699C>A GRCh38
NC_000001.10:g.53662371C>A , CM000663.1:g.53662371C>A GRCh37
NC_000001.9:g.53434959C>A NCBI36
NG_008035.1:g.5271C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-245C>A ENSP00000360541.3:n.-245C>A
NM_000098.2:c.-245C>A NP_000089.1:n.-245C>A
NM_001330589.1:c.-245C>A NP_001317518.1:n.-245C>A