Canonical Allele Identifier: CA1820609063

Gene: HHLA1

Linked Data

• dbSNP Id: rs1586731823

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132091002A>C , CM000670.2:g.132091002A>C	GRCh38
NC_000008.10:g.133103249A>C , CM000670.1:g.133103249A>C	GRCh37
NC_000008.9:g.133172431A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000414222.2:c.449-1403T>G MANE Select	ENSP00000388322.1:n.449-1403T>G
ENST00000673615.1:c.557-1403T>G	ENSP00000500443.1:n.557-1403T>G
ENST00000414222.1:c.449-1403T>G	ENSP00000388322.1:n.449-1403T>G
ENST00000434736.6:c.557-1403T>G	ENSP00000407107.2:n.557-1403T>G
NM_001145095.1:c.449-1403T>G	NP_001138567.1:n.449-1403T>G
NM_001145095.3:c.449-1403T>G MANE Select	NP_001138567.1:n.449-1403T>G