Canonical Allele Identifier: CA682974652
Gene: KLRC1 HGNC NCBI

Linked Data

dbSNP Id: rs1349586275
gnomAD v3: 12-10445881-C-T
gnomAD v4: 12-10445881-C-T
MyVariant Identifiers: chr12:g.10598480C>T (hg19) chr12:g.10445881C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10445881C>T , CM000674.2:g.10445881C>T GRCh38
NC_000012.11:g.10598480C>T , CM000674.1:g.10598480C>T GRCh37
NC_000012.10:g.10489747C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000536188.5:c.685+687G>A ENSP00000441432.1:n.685+687G>A
NM_001304448.1:c.685+687G>A NP_001291377.1:n.685+687G>A
XM_024448973.1:c.685+687G>A XP_024304741.1:n.685+687G>A
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