Canonical Allele Identifier: CA185436941
Gene: HHLA1 HGNC NCBI

Linked Data

dbSNP Id: rs2014357

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132091043T>C , CM000670.2:g.132091043T>C GRCh38
NC_000008.10:g.133103290T>C , CM000670.1:g.133103290T>C GRCh37
NC_000008.9:g.133172472T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000414222.2:c.449-1444A>G MANE Select ENSP00000388322.1:n.449-1444A>G
ENST00000673615.1:c.557-1444A>G ENSP00000500443.1:n.557-1444A>G
ENST00000414222.1:c.449-1444A>G ENSP00000388322.1:n.449-1444A>G
ENST00000434736.6:c.557-1444A>G ENSP00000407107.2:n.557-1444A>G
NM_001145095.1:c.449-1444A>G NP_001138567.1:n.449-1444A>G
NM_001145095.3:c.449-1444A>G MANE Select NP_001138567.1:n.449-1444A>G