Canonical Allele Identifier: CA847613772
Gene: HHLA1 HGNC NCBI

Linked Data

dbSNP Id: rs1158458790
MyVariant Identifiers: chr8:g.133103225C>G (hg19) chr8:g.132090978C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132090978C>G , CM000670.2:g.132090978C>G GRCh38
NC_000008.10:g.133103225C>G , CM000670.1:g.133103225C>G GRCh37
NC_000008.9:g.133172407C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000414222.2:c.449-1379G>C MANE Select ENSP00000388322.1:n.449-1379G>C
ENST00000673615.1:c.557-1379G>C ENSP00000500443.1:n.557-1379G>C
ENST00000414222.1:c.449-1379G>C ENSP00000388322.1:n.449-1379G>C
ENST00000434736.6:c.557-1379G>C ENSP00000407107.2:n.557-1379G>C
NM_001145095.1:c.449-1379G>C NP_001138567.1:n.449-1379G>C
NM_001145095.3:c.449-1379G>C MANE Select NP_001138567.1:n.449-1379G>C
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