Canonical Allele Identifier: CA2439140568
Gene: PGK1 HGNC NCBI

Linked Data

dbSNP Id: rs2078366800
gnomAD v4: X-78123413-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123413A>C , CM000685.2:g.78123413A>C GRCh38
NC_000023.10:g.77378910A>C , CM000685.1:g.77378910A>C GRCh37
NC_000023.9:g.77265566A>C NCBI36
NG_008862.1:g.24245A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.936+39A>C MANE Select ENSP00000362413.4:n.936+39A>C
ENST00000644362.1:c.852+39A>C ENSP00000496140.1:n.852+39A>C
ENST00000373316.4:c.936+39A>C ENSP00000362413.4:n.936+39A>C
NM_000291.3:c.936+39A>C NP_000282.1:n.936+39A>C
NM_000291.4:c.936+39A>C MANE Select NP_000282.1:n.936+39A>C