Canonical Allele Identifier: CA10636618

Gene: ALDH18A1

Linked Data

• ClinVar Variation Id: 301784
• ClinVar RCV Id: RCV000317435
• dbSNP Id: rs185345785
• gnomAD v2: 10-97416491-A-G
• gnomAD v3: 10-95656734-A-G
• gnomAD v4: 10-95656734-A-G
• MyVariant Identifiers: chr10:g.97416491A>G (hg19) ; chr10:g.95656734A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95656734A>G , CM000672.2:g.95656734A>G	GRCh38
NC_000010.10:g.97416491A>G , CM000672.1:g.97416491A>G	GRCh37
NC_000010.9:g.97406481A>G	NCBI36
NG_012258.1:g.5077T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001017423.1:c.-166T>C	NP_001017423.1:n.-166T>C
NM_002860.3:c.-166T>C	NP_002851.2:n.-166T>C
XM_011540001.1:c.-284T>C	XP_011538303.1:n.-284T>C
NM_001323412.1:c.-284T>C	NP_001310341.1:n.-284T>C
NM_001323413.1:c.-317T>C	NP_001310342.1:n.-317T>C
NM_001323415.1:c.-317T>C	NP_001310344.1:n.-317T>C
NM_001323416.1:c.-435T>C	NP_001310345.1:n.-435T>C
NM_001323417.1:c.-166T>C	NP_001310346.1:n.-166T>C
NM_001323418.1:c.-435T>C	NP_001310347.1:n.-435T>C
NM_001323419.1:c.-332T>C	NP_001310348.1:n.-332T>C
XM_024448094.1:c.-166T>C	XP_024303862.1:n.-166T>C
XM_024448096.1:c.-166T>C	XP_024303864.1:n.-166T>C
XM_024448097.1:c.-284T>C	XP_024303865.1:n.-284T>C