Canonical Allele Identifier: CA130121982
Gene: HAVCR2 HGNC NCBI

Linked Data

dbSNP Id: rs908780823
gnomAD v3: 5-157109386-G-A
gnomAD v4: 5-157109386-G-A
MyVariant Identifiers: chr5:g.156536397G>A (hg19) chr5:g.157109386G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157109386G>A , CM000667.2:g.157109386G>A GRCh38
NC_000005.9:g.156536397G>A , CM000667.1:g.156536397G>A GRCh37
NC_000005.8:g.156468975G>A NCBI36
NG_030444.1:g.4852C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000524219.2:c.-293-2424C>T ENSP00000430328.2:n.-293-2424C>T
ENST00000696899.1:c.-264-139C>T ENSP00000512960.1:n.-264-139C>T
ENST00000696901.1:c.-403C>T ENSP00000512962.1:n.-403C>T
ENST00000307851.8:c.-403C>T ENSP00000312002.4:n.-403C>T
ENST00000524219.1:c.-293-2424C>T ENSP00000430328.1:n.-293-2424C>T
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