Canonical Allele Identifier: CA387790609
Gene: KL HGNC NCBI

Linked Data

dbSNP Id: rs1000908514
gnomAD v4: 13-33053920-G-A
MyVariant Identifiers: chr13:g.33628057G>A (hg19) chr13:g.33053920G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.33053920G>A , CM000675.2:g.33053920G>A GRCh38
NC_000013.10:g.33628057G>A , CM000675.1:g.33628057G>A GRCh37
NC_000013.9:g.32526057G>A NCBI36
NG_011485.1:g.42487G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380099.4:c.973G>A MANE Select ENSP00000369442.3:p.Gly325Ser
ENST00000380099.3:c.973G>A ENSP00000369442.3:p.Gly325Ser
ENST00000487852.1:n.981G>A
NM_004795.3:c.973G>A NP_004786.2:p.Gly325Ser
XM_006719895.1:c.52G>A XP_006719958.1:p.Gly18Ser
XM_006719895.2:c.52G>A XP_006719958.1:p.Gly18Ser
NM_004795.4:c.973G>A MANE Select NP_004786.2:p.Gly325Ser
Search 100 bp 5'
Search 100 bp 3'