Canonical Allele Identifier: CA130121977
Gene: HAVCR2 HGNC NCBI

Linked Data

dbSNP Id: rs982962416
gnomAD v4: 5-157109374-C-T
MyVariant Identifiers: chr5:g.156536385C>T (hg19) chr5:g.157109374C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157109374C>T , CM000667.2:g.157109374C>T GRCh38
NC_000005.9:g.156536385C>T , CM000667.1:g.156536385C>T GRCh37
NC_000005.8:g.156468963C>T NCBI36
NG_030444.1:g.4864G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000524219.2:c.-293-2412G>A ENSP00000430328.2:n.-293-2412G>A
ENST00000696899.1:c.-264-127G>A ENSP00000512960.1:n.-264-127G>A
ENST00000696901.1:c.-391G>A ENSP00000512962.1:n.-391G>A
ENST00000307851.8:c.-391G>A ENSP00000312002.4:n.-391G>A
ENST00000524219.1:c.-293-2412G>A ENSP00000430328.1:n.-293-2412G>A
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