Canonical Allele Identifier: CA2687149726
Gene: HGSNAT HGNC NCBI

Linked Data

gnomAD v4: 8-43140449-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.43140449A>G , CM000670.2:g.43140449A>G GRCh38
NC_000008.10:g.42995592A>G , CM000670.1:g.42995592A>G GRCh37
NC_000008.9:g.43114749A>G NCBI36
NG_009552.1:g.5001A>G

Transcript Alleles

HGVS Amino-acid Change
NM_152419.2:c.-48A>G NP_689632.2:n.-48A>G
XM_005273409.1:c.-48A>G XP_005273466.1:n.-48A>G
XM_005273410.1:c.-48A>G XP_005273467.1:n.-48A>G
XM_005273411.1:c.-48A>G XP_005273468.1:n.-48A>G
XM_005273412.2:c.-48A>G XP_005273469.1:n.-48A>G
XM_005273412.4:c.-48A>G XP_005273469.1:n.-48A>G
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