Canonical Allele Identifier: CA2687149736
Gene: HGSNAT HGNC NCBI

Linked Data

gnomAD v4: 8-43140458-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.43140458C>A , CM000670.2:g.43140458C>A GRCh38
NC_000008.10:g.42995601C>A , CM000670.1:g.42995601C>A GRCh37
NC_000008.9:g.43114758C>A NCBI36
NG_009552.1:g.5010C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379644.8:c.-39C>A ENSP00000368965.4:n.-39C>A
NM_152419.2:c.-39C>A NP_689632.2:n.-39C>A
XM_005273409.1:c.-39C>A XP_005273466.1:n.-39C>A
XM_005273410.1:c.-39C>A XP_005273467.1:n.-39C>A
XM_005273411.1:c.-39C>A XP_005273468.1:n.-39C>A
XM_005273412.2:c.-39C>A XP_005273469.1:n.-39C>A
XM_005273412.4:c.-39C>A XP_005273469.1:n.-39C>A
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