Canonical Allele Identifier: CA409437137
Gene: PCK1 HGNC NCBI

Linked Data

gnomAD v4: 20-57565362-T-C
MyVariant Identifiers: chr20:g.56140418T>C (hg19) chr20:g.57565362T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.57565362T>C , CM000682.2:g.57565362T>C GRCh38
NC_000020.10:g.56140418T>C , CM000682.1:g.56140418T>C GRCh37
NC_000020.9:g.55573824T>C NCBI36
NG_008205.1:g.9282T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000319441.6:c.1427T>C MANE Select ENSP00000319814.4:p.Met476Thr
ENST00000319441.5:c.1427T>C ENSP00000319814.4:p.Met476Thr
ENST00000467047.1:n.4069T>C
ENST00000485958.1:n.551T>C
NM_002591.3:c.1427T>C NP_002582.3:p.Met476Thr
XM_011528839.1:c.1031T>C XP_011527141.1:p.Met344Thr
XM_024451888.1:c.1031T>C XP_024307656.1:p.Met344Thr
NM_002591.4:c.1427T>C MANE Select NP_002582.3:p.Met476Thr
Search 100 bp 5'
Search 100 bp 3'