Canonical Allele Identifier: CA682974662
Gene: KLRC1 HGNC NCBI

Linked Data

dbSNP Id: rs1379763047
MyVariant Identifiers: chr12:g.10598494G>C (hg19) chr12:g.10445895G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10445895G>C , CM000674.2:g.10445895G>C GRCh38
NC_000012.11:g.10598494G>C , CM000674.1:g.10598494G>C GRCh37
NC_000012.10:g.10489761G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000536188.5:c.685+673C>G ENSP00000441432.1:n.685+673C>G
NM_001304448.1:c.685+673C>G NP_001291377.1:n.685+673C>G
XM_024448973.1:c.685+673C>G XP_024304741.1:n.685+673C>G
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