Canonical Allele Identifier: CA91448629
Gene: MSANTD1 HGNC NCBI

Linked Data

dbSNP Id: rs191930001
gnomAD v2: 4-3258518-C-T
gnomAD v3: 4-3256791-C-T
gnomAD v4: 4-3256791-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3256791C>T , CM000666.2:g.3256791C>T GRCh38
NC_000004.11:g.3258518C>T , CM000666.1:g.3258518C>T GRCh37
NC_000004.10:g.3228316C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000505599.5:c.729+934C>T ENSP00000425405.1:n.729+934C>T
ENST00000510580.1:c.765+898C>T ENSP00000420966.1:n.765+898C>T
XM_011513464.1:c.729+934C>T XP_011511766.1:n.729+934C>T
XR_924950.1:n.753+934C>T