Canonical Allele Identifier: CA121295366

Gene: MSH3

Linked Data

• dbSNP Id: rs550630377
• gnomAD v2: 5-79971018-G-C
• gnomAD v3: 5-80675199-G-C
• gnomAD v4: 5-80675199-G-C
• MyVariant Identifiers: chr5:g.79971018G>C (hg19) ; chr5:g.80675199G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80675199G>C , CM000667.2:g.80675199G>C	GRCh38
NC_000005.9:g.79971018G>C , CM000667.1:g.79971018G>C	GRCh37
NC_000005.8:g.80006774G>C	NCBI36
NG_016607.1:g.25725G>C
NG_016607.2:g.25725G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1173+71G>C MANE Select	ENSP00000265081.6:n.1173+71G>C
ENST00000658259.1:c.1005+71G>C	ENSP00000499617.1:n.1005+71G>C
ENST00000667069.1:c.1173+71G>C	ENSP00000499502.1:n.1173+71G>C
ENST00000670357.1:c.1173+71G>C	ENSP00000499791.1:n.1173+71G>C
ENST00000265081.6:c.1173+71G>C	ENSP00000265081.6:n.1173+71G>C
NM_002439.4:c.1173+71G>C	NP_002430.3:n.1173+71G>C
NM_002439.5:c.1173+71G>C MANE Select	NP_002430.3:n.1173+71G>C