Canonical Allele Identifier: CA497678330

Linked Data

dbSNP Id: rs1433879065
gnomAD v2: 17-4836883-A-G
gnomAD v4: 17-4933588-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4933588A>G , CM000679.2:g.4933588A>G GRCh38
NC_000017.10:g.4836883A>G , CM000679.1:g.4836883A>G GRCh37
NC_000017.9:g.4777663A>G NCBI36
NG_008767.2:g.6294A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000329125.6:c.984A>G (GP1BA) MANE Select ENSP00000329380.5:p.Ser328=
ENST00000649830.1:c.-888+754T>C (CHRNE) ENSP00000496907.1:n.-888+754T>C
ENST00000329125.5:c.984A>G (GP1BA) ENSP00000329380.5:p.Ser328=
ENST00000611961.1:c.984A>G (GP1BA) ENSP00000484439.1:p.Ser328=
NM_000173.6:c.984A>G (GP1BA) NP_000164.5:p.Ser328=
NM_000173.7:c.984A>G (GP1BA) MANE Select NP_000164.5:p.Ser328=