Canonical Allele Identifier: CA445021311
Gene: CARTPT HGNC NCBI

Linked Data

dbSNP Id: rs61730984
MyVariant Identifiers: chr5:g.71015228A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719401A>C , CM000667.2:g.71719401A>C GRCh38
NC_000005.9:g.71015228A>C , CM000667.1:g.71015228A>C GRCh37
NC_000005.8:g.71050984A>C NCBI36
NG_015988.1:g.5239A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.108A>C MANE Select ENSP00000296777.4:p.Arg36=
ENST00000296777.4:c.108A>C ENSP00000296777.4:p.Arg36=
NM_004291.3:c.108A>C NP_004282.1:p.Arg36=
NM_004291.4:c.108A>C MANE Select NP_004282.1:p.Arg36=
Search 100 bp 5'
Search 100 bp 3'