Canonical Allele Identifier: CA497677042
Gene: GP1BA HGNC NCBI
CHRNE HGNC NCBI

Linked Data

COSMIC: COSM356829
MyVariant Identifiers: chr17:g.4835938C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4932643C>T , CM000679.2:g.4932643C>T GRCh38
NC_000017.10:g.4835938C>T , CM000679.1:g.4835938C>T GRCh37
NC_000017.9:g.4776718C>T NCBI36
NG_008767.2:g.5349C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.39C>T (GP1BA) MANE Select ENSP00000329380.5:p.Pro13=
ENST00000649830.1:c.-888+1699G>A (CHRNE) ENSP00000496907.1:n.-888+1699G>A
ENST00000329125.5:c.39C>T (GP1BA) ENSP00000329380.5:p.Pro13=
ENST00000611961.1:c.39C>T (GP1BA) ENSP00000484439.1:p.Pro13=
NM_000173.6:c.39C>T (GP1BA) NP_000164.5:p.Pro13=
NM_000173.7:c.39C>T (GP1BA) MANE Select NP_000164.5:p.Pro13=
Search 100 bp 5'
Search 100 bp 3'