Canonical Allele Identifier: CA3498436
Gene: ADRB2 HGNC NCBI

Linked Data

dbSNP Id: rs773717255
ExAC: 5:148207032 T / C
gnomAD v2: 5-148207032-T-C
gnomAD v3: 5-148827469-T-C
gnomAD v4: 5-148827469-T-C
MyVariant Identifiers: chr5:g.148207032T>C (hg19) chr5:g.148827469T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148827469T>C , CM000667.2:g.148827469T>C GRCh38
NC_000005.9:g.148207032T>C , CM000667.1:g.148207032T>C GRCh37
NC_000005.8:g.148187225T>C NCBI36
NG_016421.1:g.5877T>C
NG_016421.2:g.5877T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000305988.6:c.638T>C MANE Select ENSP00000305372.4:p.Val213Ala
ENST00000305988.5:c.638T>C ENSP00000305372.4:p.Val213Ala
NM_000024.5:c.638T>C NP_000015.1:p.Val213Ala
NM_000024.6:c.638T>C MANE Select NP_000015.2:p.Val213Ala
Search 100 bp 5'
Search 100 bp 3'