Canonical Allele Identifier: CA584917101
Gene: HHLA1 HGNC NCBI

Linked Data

dbSNP Id: rs1460577171
gnomAD v2: 8-133103207-C-T
gnomAD v3: 8-132090960-C-T
gnomAD v4: 8-132090960-C-T
MyVariant Identifiers: chr8:g.133103207C>T (hg19) chr8:g.132090960C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132090960C>T , CM000670.2:g.132090960C>T GRCh38
NC_000008.10:g.133103207C>T , CM000670.1:g.133103207C>T GRCh37
NC_000008.9:g.133172389C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000414222.2:c.449-1361G>A MANE Select ENSP00000388322.1:n.449-1361G>A
ENST00000673615.1:c.557-1361G>A ENSP00000500443.1:n.557-1361G>A
ENST00000414222.1:c.449-1361G>A ENSP00000388322.1:n.449-1361G>A
ENST00000434736.6:c.557-1361G>A ENSP00000407107.2:n.557-1361G>A
NM_001145095.1:c.449-1361G>A NP_001138567.1:n.449-1361G>A
NM_001145095.3:c.449-1361G>A MANE Select NP_001138567.1:n.449-1361G>A
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