Canonical Allele Identifier: CA397319461

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4933586T>A , CM000679.2:g.4933586T>A GRCh38
NC_000017.10:g.4836881T>A , CM000679.1:g.4836881T>A GRCh37
NC_000017.9:g.4777661T>A NCBI36
NG_008767.2:g.6292T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000329125.6:c.982T>A (GP1BA) MANE Select ENSP00000329380.5:p.Ser328Thr
ENST00000649830.1:c.-888+756A>T (CHRNE) ENSP00000496907.1:n.-888+756A>T
ENST00000329125.5:c.982T>A (GP1BA) ENSP00000329380.5:p.Ser328Thr
ENST00000611961.1:c.982T>A (GP1BA) ENSP00000484439.1:p.Ser328Thr
NM_000173.6:c.982T>A (GP1BA) NP_000164.5:p.Ser328Thr
NM_000173.7:c.982T>A (GP1BA) MANE Select NP_000164.5:p.Ser328Thr