Canonical Allele Identifier: CA397321029
Gene: GP1BA HGNC NCBI
CHRNE HGNC NCBI

Linked Data

dbSNP Id: rs2151108447
MyVariant Identifiers: chr17:g.4837269C>G (hg19) chr17:g.4933974C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4933974C>G , CM000679.2:g.4933974C>G GRCh38
NC_000017.10:g.4837269C>G , CM000679.1:g.4837269C>G GRCh37
NC_000017.9:g.4778010C>G NCBI36
NG_008767.2:g.6680C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.1370C>G (GP1BA) MANE Select ENSP00000329380.5:p.Thr457Ser
ENST00000649830.1:c.-888+368G>C (CHRNE) ENSP00000496907.1:n.-888+368G>C
ENST00000329125.5:c.1370C>G (GP1BA) ENSP00000329380.5:p.Thr457Ser
ENST00000611961.1:c.1292C>G (GP1BA) ENSP00000484439.1:p.Thr431Ser
NM_000173.6:c.1370C>G (GP1BA) NP_000164.5:p.Thr457Ser
NM_000173.7:c.1370C>G (GP1BA) MANE Select NP_000164.5:p.Thr457Ser
Search 100 bp 5'
Search 100 bp 3'