Canonical Allele Identifier: CA130124620
Gene: HAVCR2 HGNC NCBI

Linked Data

dbSNP Id: rs907150789
gnomAD v3: 5-157114773-G-C
gnomAD v4: 5-157114773-G-C
MyVariant Identifiers: chr5:g.156541784G>C (hg19) chr5:g.157114773G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157114773G>C , CM000667.2:g.157114773G>C GRCh38
NC_000005.9:g.156541784G>C , CM000667.1:g.156541784G>C GRCh37
NC_000005.8:g.156474362G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000524219.2:c.-293-7811C>G ENSP00000430328.2:n.-293-7811C>G
ENST00000524219.1:c.-293-7811C>G ENSP00000430328.1:n.-293-7811C>G
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