Canonical Allele Identifier: CA130122597
Gene: HAVCR2 HGNC NCBI

Linked Data

dbSNP Id: rs10053538
gnomAD v2: 5-156537510-C-T
gnomAD v3: 5-157110499-C-T
gnomAD v4: 5-157110499-C-T
MyVariant Identifiers: chr5:g.156537510C>T (hg19) chr5:g.157110499C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157110499C>T , CM000667.2:g.157110499C>T GRCh38
NC_000005.9:g.156537510C>T , CM000667.1:g.156537510C>T GRCh37
NC_000005.8:g.156470088C>T NCBI36
NG_030444.1:g.3739G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000524219.2:c.-293-3537G>A ENSP00000430328.2:n.-293-3537G>A
ENST00000696899.1:c.-264-1252G>A ENSP00000512960.1:n.-264-1252G>A
ENST00000524219.1:c.-293-3537G>A ENSP00000430328.1:n.-293-3537G>A
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