Canonical Allele Identifier: CA2495826406
Gene: MSH2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403085C= , CM000664.2:g.47403085C= GRCh38
NC_000002.11:g.47630224C= , CM000664.1:g.47630224C= GRCh37
NC_000002.10:g.47483728C= NCBI36
NG_007110.2:g.4962C= , LRG_218:g.4962C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000543555.6:c.-121C= ENSP00000442697.1:n.-121C=
ENST00000233146.6:c.-107C= ENSP00000233146.2:n.-107C=
ENST00000454849.5:c.-121C= ENSP00000411482.1:n.-121C=
ENST00000543555.5:c.-121C= ENSP00000442697.1:n.-121C=
NM_000251.2:c.-107C= , LRG_218t1:c.-107C= NP_000242.1:n.-107C=
NM_001258281.1:c.-121C= NP_001245210.1:n.-121C=
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