Canonical Allele Identifier: CA794017908
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs1170439868
MyVariant Identifiers: chr4:g.3258356T>A (hg19) chr4:g.3256629T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256629T>A , CM000666.2:g.3256629T>A GRCh38
NC_000004.11:g.3258356T>A , CM000666.1:g.3258356T>A GRCh37
NC_000004.10:g.3228154T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000505599.5:c.729+772T>A ENSP00000425405.1:n.729+772T>A
ENST00000510580.1:c.765+736T>A ENSP00000420966.1:n.765+736T>A
XM_011513464.1:c.729+772T>A XP_011511766.1:n.729+772T>A
XR_924950.1:n.753+772T>A
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