Canonical Allele Identifier: CA907871293
Gene: TRAIP HGNC NCBI

Linked Data

dbSNP Id: rs1410668108
gnomAD v3: 3-49828778-A-G
gnomAD v4: 3-49828778-A-G
MyVariant Identifiers: chr3:g.49866211A>G (hg19) chr3:g.49828778A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828778A>G , CM000665.2:g.49828778A>G GRCh38
NC_000003.11:g.49866211A>G , CM000665.1:g.49866211A>G GRCh37
NC_000003.10:g.49841215A>G NCBI36
NG_046695.1:g.32782T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000331456.7:c.*325T>C MANE Select ENSP00000328203.2:n.*325T>C
ENST00000331456.6:c.*325T>C ENSP00000328203.2:n.*325T>C
ENST00000491060.1:n.889T>C
NM_005879.2:c.*325T>C NP_005870.2:n.*325T>C
XM_011533264.1:c.*325T>C XP_011531566.1:n.*325T>C
XM_017005526.1:c.*325T>C XP_016861015.1:n.*325T>C
XR_001739979.1:n.1939T>C
NM_005879.3:c.*325T>C MANE Select NP_005870.2:n.*325T>C
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