Canonical Allele Identifier: CA1558564005
Gene: MSH3 HGNC NCBI

Linked Data

dbSNP Id: rs1746248187
gnomAD v4: 5-80873035-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80873035G>A , CM000667.2:g.80873035G>A GRCh38
NC_000005.9:g.80168854G>A , CM000667.1:g.80168854G>A GRCh37
NC_000005.8:g.80204610G>A NCBI36
NG_016607.1:g.223561G>A
NG_016607.2:g.223561G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.3131-81G>A MANE Select ENSP00000265081.6:n.3131-81G>A
ENST00000658259.1:c.2963-81G>A ENSP00000499617.1:n.2963-81G>A
ENST00000659302.1:c.539-81G>A
ENST00000667069.1:c.2936-81G>A ENSP00000499502.1:n.2936-81G>A
ENST00000670357.1:c.*455-81G>A ENSP00000499791.1:n.*455-81G>A
ENST00000265081.6:c.3131-81G>A ENSP00000265081.6:n.3131-81G>A
NM_002439.4:c.3131-81G>A NP_002430.3:n.3131-81G>A
NM_002439.5:c.3131-81G>A MANE Select NP_002430.3:n.3131-81G>A
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