Canonical Allele Identifier: CA1167208750

Gene: CPT2

Linked Data

• dbSNP Id: rs1353601030

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.53196678G>C , CM000663.2:g.53196678G>C	GRCh38
NC_000001.10:g.53662350G>C , CM000663.1:g.53662350G>C	GRCh37
NC_000001.9:g.53434938G>C	NCBI36
NG_008035.1:g.5250G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371486.3:c.-266G>C	ENSP00000360541.3:n.-266G>C
NM_000098.2:c.-266G>C	NP_000089.1:n.-266G>C
NM_001330589.1:c.-266G>C	NP_001317518.1:n.-266G>C