Canonical Allele Identifier: CA2674442902
Gene: MSH3 HGNC NCBI

Linked Data

gnomAD v4: 5-80674878-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80674878C>A , CM000667.2:g.80674878C>A GRCh38
NC_000005.9:g.79970697C>A , CM000667.1:g.79970697C>A GRCh37
NC_000005.8:g.80006453C>A NCBI36
NG_016607.1:g.25404C>A
NG_016607.2:g.25404C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.1028-105C>A MANE Select ENSP00000265081.6:n.1028-105C>A
ENST00000658259.1:c.860-105C>A ENSP00000499617.1:n.860-105C>A
ENST00000667069.1:c.1028-105C>A ENSP00000499502.1:n.1028-105C>A
ENST00000670357.1:c.1028-105C>A ENSP00000499791.1:n.1028-105C>A
ENST00000265081.6:c.1028-105C>A ENSP00000265081.6:n.1028-105C>A
NM_002439.4:c.1028-105C>A NP_002430.3:n.1028-105C>A
NM_002439.5:c.1028-105C>A MANE Select NP_002430.3:n.1028-105C>A
Search 100 bp 5'
Search 100 bp 3'