Canonical Allele Identifier: CA563960680
Gene: ADRB2 HGNC NCBI

Linked Data

dbSNP Id: rs1195969974
gnomAD v2: 5-148206362-C-T
MyVariant Identifiers: chr5:g.148206362C>T (hg19) chr5:g.148826799C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148826799C>T , CM000667.2:g.148826799C>T GRCh38
NC_000005.9:g.148206362C>T , CM000667.1:g.148206362C>T GRCh37
NC_000005.8:g.148186555C>T NCBI36
NG_016421.1:g.5207C>T
NG_016421.2:g.5207C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000305988.6:c.-33C>T MANE Select ENSP00000305372.4:n.-33C>T
ENST00000305988.5:c.-33C>T ENSP00000305372.4:n.-33C>T
NM_000024.5:c.-33C>T NP_000015.1:n.-33C>T
NM_000024.6:c.-33C>T MANE Select NP_000015.2:n.-33C>T
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