Canonical Allele Identifier: CA2495826408
Gene: MSH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403086G= , CM000664.2:g.47403086G= GRCh38
NC_000002.11:g.47630225G= , CM000664.1:g.47630225G= GRCh37
NC_000002.10:g.47483729G= NCBI36
NG_007110.2:g.4963G= , LRG_218:g.4963G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000543555.6:c.-120G= ENSP00000442697.1:n.-120G=
ENST00000233146.6:c.-106G= ENSP00000233146.2:n.-106G=
ENST00000454849.5:c.-120G= ENSP00000411482.1:n.-120G=
ENST00000543555.5:c.-120G= ENSP00000442697.1:n.-120G=
NM_000251.2:c.-106G= , LRG_218t1:c.-106G= NP_000242.1:n.-106G=
NM_001258281.1:c.-120G= NP_001245210.1:n.-120G=
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