Canonical Allele Identifier: CA2481224685
Gene: PKLR HGNC NCBI

Linked Data

dbSNP Id: rs1674471942
gnomAD v4: 1-155290244-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155290244C>T , CM000663.2:g.155290244C>T GRCh38
NC_000001.10:g.155260035C>T , CM000663.1:g.155260035C>T GRCh37
NC_000001.9:g.153526659C>T NCBI36
NG_011677.1:g.16191G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000342741.6:c.*328G>A MANE Select ENSP00000339933.4:n.*328G>A
ENST00000392414.7:c.*328G>A ENSP00000376214.3:n.*328G>A
NM_000298.5:c.*328G>A NP_000289.1:n.*328G>A
NM_181871.3:c.*328G>A NP_870986.1:n.*328G>A
NM_000298.6:c.*328G>A MANE Select NP_000289.1:n.*328G>A
NM_181871.4:c.*328G>A NP_870986.1:n.*328G>A
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