Canonical Allele Identifier: CA130816915

Gene: ADRA1B

Linked Data

• dbSNP Id: rs193274872
• gnomAD v2: 5-159360419-A-C
• gnomAD v3: 5-159933412-A-C
• gnomAD v4: 5-159933412-A-C
• MyVariant Identifiers: chr5:g.159360419A>C (hg19) ; chr5:g.159933412A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159933412A>C , CM000667.2:g.159933412A>C	GRCh38
NC_000005.9:g.159360419A>C , CM000667.1:g.159360419A>C	GRCh37
NC_000005.8:g.159292997A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306675.5:c.949+15558A>C MANE Select	ENSP00000306662.3:n.949+15558A>C
ENST00000306675.3:c.949+15558A>C	ENSP00000306662.3:n.949+15558A>C
NM_000679.3:c.949+15558A>C	NP_000670.1:n.949+15558A>C
XM_005265818.2:c.950-14278A>C	XP_005265875.1:n.950-14278A>C
XM_005265819.2:c.949+15558A>C	XP_005265876.1:n.949+15558A>C
XM_006714821.2:c.949+15558A>C	XP_006714884.1:n.949+15558A>C
XM_011534435.1:c.1057+7816A>C	XP_011532737.1:n.1057+7816A>C
XM_011534436.1:c.1057+7816A>C	XP_011532738.1:n.1057+7816A>C
XM_011534437.1:c.1057+7816A>C	XP_011532739.1:n.1057+7816A>C
XM_011534439.1:c.1057+7816A>C	XP_011532741.1:n.1057+7816A>C
XM_005265818.3:c.950-14278A>C	XP_005265875.1:n.950-14278A>C
XM_006714821.3:c.949+15558A>C	XP_006714884.1:n.949+15558A>C
XM_011534437.2:c.1057+7816A>C	XP_011532739.1:n.1057+7816A>C
NM_000679.4:c.949+15558A>C MANE Select	NP_000670.1:n.949+15558A>C