Canonical Allele Identifier: CA1434131037
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs1722405157
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256693C>T , CM000666.2:g.3256693C>T GRCh38
NC_000004.11:g.3258420C>T , CM000666.1:g.3258420C>T GRCh37
NC_000004.10:g.3228218C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000505599.5:c.729+836C>T ENSP00000425405.1:n.729+836C>T
ENST00000510580.1:c.765+800C>T ENSP00000420966.1:n.765+800C>T
XM_011513464.1:c.729+836C>T XP_011511766.1:n.729+836C>T
XR_924950.1:n.753+836C>T
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