Canonical Allele Identifier: CA11949447
Gene: HAVCR1 HGNC NCBI

Linked Data

dbSNP Id: rs41297579
gnomAD v2: 5-156486408-C-T
gnomAD v3: 5-157059397-C-T
gnomAD v4: 5-157059397-C-T
MyVariant Identifiers: chr5:g.156486408C>T (hg19) chr5:g.157059397C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157059397C>T , CM000667.2:g.157059397C>T GRCh38
NC_000005.9:g.156486408C>T , CM000667.1:g.156486408C>T GRCh37
NC_000005.8:g.156418986C>T NCBI36
NG_017001.1:g.4563G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000699093.1:c.-12-1442G>A ENSP00000514125.1:n.-12-1442G>A
XM_011534511.1:c.-133-1321G>A XP_011532813.1:n.-133-1321G>A
XM_011534513.1:c.-12-1442G>A XP_011532815.1:n.-12-1442G>A
XM_024446020.1:c.-136-1318G>A XP_024301788.1:n.-136-1318G>A
XM_024446021.1:c.-133-1321G>A XP_024301789.1:n.-133-1321G>A
XM_024446023.1:c.-12-1442G>A XP_024301791.1:n.-12-1442G>A
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