Canonical Allele Identifier: CA1630834340
Gene: MSH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403074T= , CM000664.2:g.47403074T= GRCh38
NC_000002.11:g.47630213T= , CM000664.1:g.47630213T= GRCh37
NC_000002.10:g.47483717T= NCBI36
NG_007110.2:g.4951T= , LRG_218:g.4951T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000543555.6:c.-132T= ENSP00000442697.1:n.-132T=
ENST00000233146.6:c.-118T= ENSP00000233146.2:n.-118T=
ENST00000454849.5:c.-132T= ENSP00000411482.1:n.-132T=
ENST00000543555.5:c.-132T= ENSP00000442697.1:n.-132T=
NM_000251.2:c.-118T= , LRG_218t1:c.-118T= NP_000242.1:n.-118T=
NM_001258281.1:c.-132T= NP_001245210.1:n.-132T=
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