Canonical Allele Identifier: CA2694156103
Gene: PGK1 HGNC NCBI

Linked Data

gnomAD v4: X-78123045-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123045T>C , CM000685.2:g.78123045T>C GRCh38
NC_000023.10:g.77378542T>C , CM000685.1:g.77378542T>C GRCh37
NC_000023.9:g.77265198T>C NCBI36
NG_008862.1:g.23877T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.756+96T>C MANE Select ENSP00000362413.4:n.756+96T>C
ENST00000644362.1:c.672+96T>C ENSP00000496140.1:n.672+96T>C
ENST00000373316.4:c.756+96T>C ENSP00000362413.4:n.756+96T>C
ENST00000474281.1:n.163+44T>C
NM_000291.3:c.756+96T>C NP_000282.1:n.756+96T>C
NM_000291.4:c.756+96T>C MANE Select NP_000282.1:n.756+96T>C