Canonical Allele Identifier: CA813669952
Gene: CARTPT HGNC NCBI

Linked Data

dbSNP Id: rs1330145899
MyVariant Identifiers: chr5:g.71015076A>C (hg19) chr5:g.71719249A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719249A>C , CM000667.2:g.71719249A>C GRCh38
NC_000005.9:g.71015076A>C , CM000667.1:g.71015076A>C GRCh37
NC_000005.8:g.71050832A>C NCBI36
NG_015988.1:g.5087A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.4:c.-45A>C ENSP00000296777.4:n.-45A>C
NM_004291.3:c.-45A>C NP_004282.1:n.-45A>C
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