Canonical Allele Identifier: CA447434353
Gene: HAVCR2 HGNC NCBI

Linked Data

dbSNP Id: rs1454168969
gnomAD v3: 5-157114796-T-G
gnomAD v4: 5-157114796-T-G
MyVariant Identifiers: chr5:g.156541807T>G (hg19) chr5:g.157114796T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157114796T>G , CM000667.2:g.157114796T>G GRCh38
NC_000005.9:g.156541807T>G , CM000667.1:g.156541807T>G GRCh37
NC_000005.8:g.156474385T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000524219.2:c.-293-7834A>C ENSP00000430328.2:n.-293-7834A>C
ENST00000524219.1:c.-293-7834A>C ENSP00000430328.1:n.-293-7834A>C
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