Canonical Allele Identifier: CA736875849
Gene: CPT2 HGNC NCBI

Linked Data

dbSNP Id: rs892801392
MyVariant Identifiers: chr1:g.53662366G>T (hg19) chr1:g.53196694G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53196694G>T , CM000663.2:g.53196694G>T GRCh38
NC_000001.10:g.53662366G>T , CM000663.1:g.53662366G>T GRCh37
NC_000001.9:g.53434954G>T NCBI36
NG_008035.1:g.5266G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371486.3:c.-250G>T ENSP00000360541.3:n.-250G>T
NM_000098.2:c.-250G>T NP_000089.1:n.-250G>T
NM_001330589.1:c.-250G>T NP_001317518.1:n.-250G>T
Search 100 bp 5'
Search 100 bp 3'