Canonical Allele Identifier: CA497677688
Gene: GP1BA HGNC NCBI
CHRNE HGNC NCBI

Linked Data

dbSNP Id: rs1304181767
gnomAD v2: 17-4836505-A-C
gnomAD v4: 17-4933210-A-C
MyVariant Identifiers: chr17:g.4836505A>C (hg19) chr17:g.4933210A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4933210A>C , CM000679.2:g.4933210A>C GRCh38
NC_000017.10:g.4836505A>C , CM000679.1:g.4836505A>C GRCh37
NC_000017.9:g.4777285A>C NCBI36
NG_008767.2:g.5916A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.606A>C (GP1BA) MANE Select ENSP00000329380.5:p.Thr202=
ENST00000649830.1:c.-888+1132T>G (CHRNE) ENSP00000496907.1:n.-888+1132T>G
ENST00000329125.5:c.606A>C (GP1BA) ENSP00000329380.5:p.Thr202=
ENST00000611961.1:c.606A>C (GP1BA) ENSP00000484439.1:p.Thr202=
NM_000173.6:c.606A>C (GP1BA) NP_000164.5:p.Thr202=
NM_000173.7:c.606A>C (GP1BA) MANE Select NP_000164.5:p.Thr202=
Search 100 bp 5'
Search 100 bp 3'