Canonical Allele Identifier: CA3298276
Gene: CARTPT HGNC NCBI

Linked Data

dbSNP Id: rs61730984
ExAC: 5:71015228 A / G
gnomAD v2: 5-71015228-A-G
gnomAD v3: 5-71719401-A-G
gnomAD v4: 5-71719401-A-G
MyVariant Identifiers: chr5:g.71015228A>G (hg19) chr5:g.71719401A>G (hg38)
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Genomic Alleles

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

Transcript Alleles

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