Canonical Allele Identifier: CA130124621
Gene: HAVCR2 HGNC NCBI

Linked Data

dbSNP Id: rs993005973
gnomAD v2: 5-156541805-C-T
gnomAD v3: 5-157114794-C-T
gnomAD v4: 5-157114794-C-T
MyVariant Identifiers: chr5:g.156541805C>T (hg19) chr5:g.157114794C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157114794C>T , CM000667.2:g.157114794C>T GRCh38
NC_000005.9:g.156541805C>T , CM000667.1:g.156541805C>T GRCh37
NC_000005.8:g.156474383C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000524219.2:c.-293-7832G>A ENSP00000430328.2:n.-293-7832G>A
ENST00000524219.1:c.-293-7832G>A ENSP00000430328.1:n.-293-7832G>A
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