Canonical Allele Identifier: CA130124630
Gene: HAVCR2 HGNC NCBI

Linked Data

dbSNP Id: rs948960961
gnomAD v2: 5-156541835-G-A
gnomAD v3: 5-157114824-G-A
gnomAD v4: 5-157114824-G-A
MyVariant Identifiers: chr5:g.156541835G>A (hg19) chr5:g.157114824G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157114824G>A , CM000667.2:g.157114824G>A GRCh38
NC_000005.9:g.156541835G>A , CM000667.1:g.156541835G>A GRCh37
NC_000005.8:g.156474413G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000524219.2:c.-293-7862C>T ENSP00000430328.2:n.-293-7862C>T
ENST00000524219.1:c.-293-7862C>T ENSP00000430328.1:n.-293-7862C>T
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