Canonical Allele Identifier: CA130122694
Gene: HAVCR2 HGNC NCBI

Linked Data

dbSNP Id: rs542688283
gnomAD v3: 5-157110684-C-T
gnomAD v4: 5-157110684-C-T
MyVariant Identifiers: chr5:g.156537695C>T (hg19) chr5:g.157110684C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157110684C>T , CM000667.2:g.157110684C>T GRCh38
NC_000005.9:g.156537695C>T , CM000667.1:g.156537695C>T GRCh37
NC_000005.8:g.156470273C>T NCBI36
NG_030444.1:g.3554G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000524219.2:c.-293-3722G>A ENSP00000430328.2:n.-293-3722G>A
ENST00000696899.1:c.-264-1437G>A ENSP00000512960.1:n.-264-1437G>A
ENST00000524219.1:c.-293-3722G>A ENSP00000430328.1:n.-293-3722G>A
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