Canonical Allele Identifier: CA130121959
Gene: HAVCR2 HGNC NCBI

Linked Data

dbSNP Id: rs1024742749
MyVariant Identifiers: chr5:g.156536316T>C (hg19) chr5:g.157109305T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157109305T>C , CM000667.2:g.157109305T>C GRCh38
NC_000005.9:g.156536316T>C , CM000667.1:g.156536316T>C GRCh37
NC_000005.8:g.156468894T>C NCBI36
NG_030444.1:g.4933A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000524219.2:c.-293-2343A>G ENSP00000430328.2:n.-293-2343A>G
ENST00000696899.1:c.-264-58A>G ENSP00000512960.1:n.-264-58A>G
ENST00000696901.1:c.-322A>G ENSP00000512962.1:n.-322A>G
ENST00000307851.8:c.-322A>G ENSP00000312002.4:n.-322A>G
ENST00000524219.1:c.-293-2343A>G ENSP00000430328.1:n.-293-2343A>G
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