Canonical Allele Identifier: CA560552881
Gene: MSH3 HGNC NCBI

Linked Data

dbSNP Id: rs1229912181
gnomAD v2: 5-79970717-G-A
gnomAD v3: 5-80674898-G-A
gnomAD v4: 5-80674898-G-A
MyVariant Identifiers: chr5:g.79970717G>A (hg19) chr5:g.80674898G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80674898G>A , CM000667.2:g.80674898G>A GRCh38
NC_000005.9:g.79970717G>A , CM000667.1:g.79970717G>A GRCh37
NC_000005.8:g.80006473G>A NCBI36
NG_016607.1:g.25424G>A
NG_016607.2:g.25424G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.1028-85G>A MANE Select ENSP00000265081.6:n.1028-85G>A
ENST00000658259.1:c.860-85G>A ENSP00000499617.1:n.860-85G>A
ENST00000667069.1:c.1028-85G>A ENSP00000499502.1:n.1028-85G>A
ENST00000670357.1:c.1028-85G>A ENSP00000499791.1:n.1028-85G>A
ENST00000265081.6:c.1028-85G>A ENSP00000265081.6:n.1028-85G>A
NM_002439.4:c.1028-85G>A NP_002430.3:n.1028-85G>A
NM_002439.5:c.1028-85G>A MANE Select NP_002430.3:n.1028-85G>A
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