Canonical Allele Identifier: CA287215352
Gene: GP1BA HGNC NCBI
CHRNE HGNC NCBI

Linked Data

dbSNP Id: rs2243109
gnomAD v2: 17-4835693-G-A
gnomAD v3: 17-4932398-G-A
gnomAD v4: 17-4932398-G-A
MyVariant Identifiers: chr17:g.4835693G>A (hg19) chr17:g.4932398G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4932398G>A , CM000679.2:g.4932398G>A GRCh38
NC_000017.10:g.4835693G>A , CM000679.1:g.4835693G>A GRCh37
NC_000017.9:g.4776473G>A NCBI36
NG_008767.2:g.5104G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.-7+33G>A (GP1BA) MANE Select ENSP00000329380.5:n.-7+33G>A
ENST00000649830.1:c.-888+1944C>T (CHRNE) ENSP00000496907.1:n.-888+1944C>T
ENST00000329125.5:c.-7+33G>A (GP1BA) ENSP00000329380.5:n.-7+33G>A
ENST00000611961.1:c.-7+33G>A (GP1BA) ENSP00000484439.1:n.-7+33G>A
NM_000173.6:c.-7+33G>A (GP1BA) NP_000164.5:n.-7+33G>A
NM_000173.7:c.-7+33G>A (GP1BA) MANE Select NP_000164.5:n.-7+33G>A
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