Canonical Allele Identifier: CA2591399242
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs2110325107
gnomAD v3: 4-3256757-G-C
gnomAD v4: 4-3256757-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256757G>C , CM000666.2:g.3256757G>C GRCh38
NC_000004.11:g.3258484G>C , CM000666.1:g.3258484G>C GRCh37
NC_000004.10:g.3228282G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+900G>C ENSP00000425405.1:n.729+900G>C
ENST00000510580.1:c.765+864G>C ENSP00000420966.1:n.765+864G>C
XM_011513464.1:c.729+900G>C XP_011511766.1:n.729+900G>C
XR_924950.1:n.753+900G>C
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