Canonical Allele Identifier: CA130122657
Gene: HAVCR2 HGNC NCBI

Linked Data

dbSNP Id: rs200181745
gnomAD v2: 5-156537616-T-G
gnomAD v3: 5-157110605-T-G
gnomAD v4: 5-157110605-T-G
MyVariant Identifiers: chr5:g.156537616T>G (hg19) chr5:g.157110605T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157110605T>G , CM000667.2:g.157110605T>G GRCh38
NC_000005.9:g.156537616T>G , CM000667.1:g.156537616T>G GRCh37
NC_000005.8:g.156470194T>G NCBI36
NG_030444.1:g.3633A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000524219.2:c.-293-3643A>C ENSP00000430328.2:n.-293-3643A>C
ENST00000696899.1:c.-264-1358A>C ENSP00000512960.1:n.-264-1358A>C
ENST00000524219.1:c.-293-3643A>C ENSP00000430328.1:n.-293-3643A>C
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