Canonical Allele Identifier: CA2674445884
Gene: MSH3 HGNC NCBI

Linked Data

gnomAD v4: 5-80873018-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80873018C>A , CM000667.2:g.80873018C>A GRCh38
NC_000005.9:g.80168837C>A , CM000667.1:g.80168837C>A GRCh37
NC_000005.8:g.80204593C>A NCBI36
NG_016607.1:g.223544C>A
NG_016607.2:g.223544C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000265081.7:c.3131-98C>A MANE Select ENSP00000265081.6:n.3131-98C>A
ENST00000658259.1:c.2963-98C>A ENSP00000499617.1:n.2963-98C>A
ENST00000659302.1:c.539-98C>A
ENST00000667069.1:c.2936-98C>A ENSP00000499502.1:n.2936-98C>A
ENST00000670357.1:c.*455-98C>A ENSP00000499791.1:n.*455-98C>A
ENST00000265081.6:c.3131-98C>A ENSP00000265081.6:n.3131-98C>A
NM_002439.4:c.3131-98C>A NP_002430.3:n.3131-98C>A
NM_002439.5:c.3131-98C>A MANE Select NP_002430.3:n.3131-98C>A
Search 100 bp 5'
Search 100 bp 3'