Canonical Allele Identifier: CA2639297957
Gene: SMARCD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63832088C>A , CM000679.2:g.63832088C>A GRCh38
NC_000017.10:g.61909448C>A , CM000679.1:g.61909448C>A GRCh37
NC_000017.9:g.59263180C>A NCBI36
NG_053004.1:g.15904G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000448276.7:c.*850G>T MANE Select ENSP00000392617.2:n.*850G>T
ENST00000448276.6:c.*850G>T ENSP00000392617.2:n.*850G>T
ENST00000613943.4:c.2335G>T ENSP00000483605.1:n.2335G>T
NM_001098426.1:c.*850G>T NP_001091896.1:n.*850G>T
XM_005257604.2:c.*850G>T XP_005257661.2:n.*850G>T
NM_001330439.1:c.*850G>T NP_001317368.1:n.*850G>T
NM_001330440.1:c.*850G>T NP_001317369.1:n.*850G>T
NM_001098426.2:c.*850G>T MANE Select NP_001091896.1:n.*850G>T
NM_001330440.2:c.*850G>T NP_001317369.1:n.*850G>T