Canonical Allele Identifier: CA10300765
Gene: ALG12 HGNC NCBI

Linked Data

dbSNP Id: rs758398852
ExAC: 22:50307423 T / A
gnomAD v2: 22-50307423-T-A
gnomAD v3: 22-49913775-T-A
gnomAD v4: 22-49913775-T-A
MyVariant Identifiers: chr22:g.50307423T>A (hg19) chr22:g.49913775T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.49913775T>A , CM000684.2:g.49913775T>A GRCh38
NC_000022.10:g.50307423T>A , CM000684.1:g.50307423T>A GRCh37
NC_000022.9:g.48693427T>A NCBI36
NG_008927.1:g.9684A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000330817.11:c.-10A>T MANE Select ENSP00000333813.5:n.-10A>T
ENST00000330817.10:c.-10A>T ENSP00000333813.5:n.-10A>T
NM_024105.3:c.-10A>T NP_077010.1:n.-10A>T
XM_011530369.1:c.-10A>T XP_011528671.1:n.-10A>T
XM_011530370.1:c.-10A>T XP_011528672.1:n.-10A>T
XM_011530371.1:c.-10A>T XP_011528673.1:n.-10A>T
XM_011530371.2:c.-10A>T XP_011528673.1:n.-10A>T
XM_017028936.1:c.-10A>T XP_016884425.1:n.-10A>T
XM_017028937.1:c.-10A>T XP_016884426.1:n.-10A>T
NM_024105.4:c.-10A>T MANE Select NP_077010.1:n.-10A>T
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