Canonical Allele Identifier: CA497678058
Gene: GP1BA HGNC NCBI
CHRNE HGNC NCBI

Linked Data

dbSNP Id: rs1172798146
COSMIC: COSM6339732
MyVariant Identifiers: chr17:g.4837192C>T (hg19) chr17:g.4933897C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4933897C>T , CM000679.2:g.4933897C>T GRCh38
NC_000017.10:g.4837192C>T , CM000679.1:g.4837192C>T GRCh37
NG_008767.2:g.6603C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.1293C>T (GP1BA) MANE Select ENSP00000329380.5:p.Ala431=
ENST00000649830.1:c.-888+445G>A (CHRNE) ENSP00000496907.1:n.-888+445G>A
ENST00000329125.5:c.1293C>T (GP1BA) ENSP00000329380.5:p.Ala431=
ENST00000611961.1:c.1272+21C>T (GP1BA) ENSP00000484439.1:n.1272+21C>T
NM_000173.6:c.1293C>T (GP1BA) NP_000164.5:p.Ala431=
NM_000173.7:c.1293C>T (GP1BA) MANE Select NP_000164.5:p.Ala431=
Search 100 bp 5'
Search 100 bp 3'