Canonical Allele Identifier: CA1554416979
Gene: CARTPT HGNC NCBI

Linked Data

dbSNP Id: rs1748664475
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719578C>T , CM000667.2:g.71719578C>T GRCh38
NC_000005.9:g.71015405C>T , CM000667.1:g.71015405C>T GRCh37
NC_000005.8:g.71051161C>T NCBI36
NG_015988.1:g.5416C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000296777.5:c.159+126C>T MANE Select ENSP00000296777.4:n.159+126C>T
ENST00000296777.4:c.159+126C>T ENSP00000296777.4:n.159+126C>T
NM_004291.3:c.159+126C>T NP_004282.1:n.159+126C>T
NM_004291.4:c.159+126C>T MANE Select NP_004282.1:n.159+126C>T
Search 100 bp 5'
Search 100 bp 3'