Canonical Allele Identifier: CA649636248
Gene: CARTPT HGNC NCBI

Linked Data

COSMIC: COSN26482057
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719257A>T , CM000667.2:g.71719257A>T GRCh38
NC_000005.9:g.71015084A>T , CM000667.1:g.71015084A>T GRCh37
NC_000005.8:g.71050840A>T NCBI36
NG_015988.1:g.5095A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.4:c.-37A>T ENSP00000296777.4:n.-37A>T
NM_004291.3:c.-37A>T NP_004282.1:n.-37A>T
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