Canonical Allele Identifier: CA378448930
Gene: ADRB1 HGNC NCBI

Linked Data

dbSNP Id: rs1847542788
gnomAD v3: 10-114045136-T-G
gnomAD v4: 10-114045136-T-G
MyVariant Identifiers: chr10:g.115804895T>G (hg19) chr10:g.114045136T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.114045136T>G , CM000672.2:g.114045136T>G GRCh38
NC_000010.10:g.115804895T>G , CM000672.1:g.115804895T>G GRCh37
NC_000010.9:g.115794885T>G NCBI36
NG_012187.1:g.6090T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369295.4:c.1004T>G MANE Select ENSP00000358301.2:p.Leu335Arg
ENST00000369295.3:c.1004T>G ENSP00000358301.2:p.Leu335Arg
NM_000684.2:c.1004T>G NP_000675.1:p.Leu335Arg
NM_000684.3:c.1004T>G MANE Select NP_000675.1:p.Leu335Arg
Search 100 bp 5'
Search 100 bp 3'