Canonical Allele Identifier: CA497678101

Linked Data

MyVariant Identifiers: chr17:g.4837207C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4933912C>G , CM000679.2:g.4933912C>G GRCh38
NC_000017.10:g.4837207C>G , CM000679.1:g.4837207C>G GRCh37
NG_008767.2:g.6618C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.1308C>G (GP1BA) MANE Select ENSP00000329380.5:p.Thr436=
ENST00000649830.1:c.-888+430G>C (CHRNE) ENSP00000496907.1:n.-888+430G>C
ENST00000329125.5:c.1308C>G (GP1BA) ENSP00000329380.5:p.Thr436=
ENST00000611961.1:c.1272+36C>G (GP1BA) ENSP00000484439.1:n.1272+36C>G
NM_000173.6:c.1308C>G (GP1BA) NP_000164.5:p.Thr436=
NM_000173.7:c.1308C>G (GP1BA) MANE Select NP_000164.5:p.Thr436=