Canonical Allele Identifier: CA466225516

Gene: AUH

Linked Data

• ClinVar Variation Id: 1695255
• ClinVar RCV Id: RCV002263505
• dbSNP Id: rs781471363
• gnomAD v2: 9-93983105-C-G
• gnomAD v3: 9-91220823-C-G
• gnomAD v4: 9-91220823-C-G
• MyVariant Identifiers: chr9:g.93983105C>G (hg19) ; chr9:g.91220823C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91220823C>G , CM000671.2:g.91220823C>G	GRCh38
NC_000009.11:g.93983105C>G , CM000671.1:g.93983105C>G	GRCh37
NC_000009.10:g.93022926C>G	NCBI36
NG_008017.1:g.146102G>C , LRG_449:g.146102G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375731.9:c.825G>C MANE Select	ENSP00000364883.5:p.Ala275=
ENST00000303617.5:c.738G>C	ENSP00000307334.5:p.Ala246=
ENST00000375731.8:c.825G>C	ENSP00000364883.4:p.Ala275=
ENST00000473695.1:n.97G>C
NM_001306190.1:c.738G>C	NP_001293119.1:p.Ala246=
NM_001698.2:c.825G>C , LRG_449t1:c.825G>C	NP_001689.1:p.Ala275=
XM_005252066.2:c.855G>C	XP_005252123.1:p.Ala285=
XM_005252067.3:c.855G>C	XP_005252124.1:p.Ala285=
XM_005252069.3:c.855G>C	XP_005252126.1:p.Ala285=
XM_005252073.2:c.363G>C	XP_005252130.1:p.Ala121=
XM_006717150.2:c.768G>C	XP_006717213.1:p.Ala256=
XM_011518801.1:c.501G>C	XP_011517103.1:p.Ala167=
XM_011518802.1:c.498G>C	XP_011517104.1:p.Ala166=
NM_001351431.1:c.498G>C	NP_001338360.1:p.Ala166=
NM_001351432.1:c.498G>C	NP_001338361.1:p.Ala166=
NM_001351433.1:c.498G>C	NP_001338362.1:p.Ala166=
XM_005252066.3:c.855G>C	XP_005252123.1:p.Ala285=
XM_005252067.4:c.855G>C	XP_005252124.1:p.Ala285=
XM_005252069.4:c.855G>C	XP_005252126.1:p.Ala285=
XM_006717150.3:c.768G>C	XP_006717213.1:p.Ala256=
XM_017014849.1:c.825G>C	XP_016870338.1:p.Ala275=
XR_001746328.2:n.1050G>C
XR_001746329.2:n.1002G>C
NM_001698.3:c.825G>C MANE Select	NP_001689.1:p.Ala275=
NM_001306190.2:c.738G>C	NP_001293119.1:p.Ala246=
NM_001351431.2:c.498G>C	NP_001338360.1:p.Ala166=
NM_001351432.2:c.498G>C	NP_001338361.1:p.Ala166=
NM_001351433.2:c.498G>C	NP_001338362.1:p.Ala166=