Canonical Allele Identifier: CA2639298169
Gene: SMARCD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63832245G>A , CM000679.2:g.63832245G>A GRCh38
NC_000017.10:g.61909605G>A , CM000679.1:g.61909605G>A GRCh37
NC_000017.9:g.59263337G>A NCBI36
NG_053004.1:g.15747C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000584483.6:n.2568C>T
ENST00000697953.1:n.3141C>T
ENST00000698013.1:n.3253C>T
ENST00000698014.1:n.3476C>T
ENST00000698015.1:n.2569C>T
ENST00000698016.1:c.*693C>T ENSP00000513502.1:n.*693C>T
ENST00000698017.1:n.2643C>T
ENST00000698018.1:n.2774C>T
ENST00000698019.1:n.2972C>T
ENST00000698020.1:n.2078C>T
ENST00000698021.1:c.1987C>T
ENST00000698022.1:c.*693C>T ENSP00000513504.1:n.*693C>T
ENST00000698023.1:n.2672C>T
ENST00000698024.1:n.2534C>T
ENST00000698025.1:n.2694C>T
ENST00000698026.1:n.1585C>T
ENST00000698027.1:c.*910C>T ENSP00000513505.1:n.*910C>T
ENST00000698028.1:n.2777C>T
ENST00000448276.7:c.*693C>T MANE Select ENSP00000392617.2:n.*693C>T
ENST00000448276.6:c.*693C>T ENSP00000392617.2:n.*693C>T
ENST00000613943.4:c.2178C>T ENSP00000483605.1:n.2178C>T
NM_001098426.1:c.*693C>T NP_001091896.1:n.*693C>T
XM_005257604.2:c.*693C>T XP_005257661.2:n.*693C>T
NM_001330439.1:c.*693C>T NP_001317368.1:n.*693C>T
NM_001330440.1:c.*693C>T NP_001317369.1:n.*693C>T
NM_001098426.2:c.*693C>T MANE Select NP_001091896.1:n.*693C>T
NM_001330440.2:c.*693C>T NP_001317369.1:n.*693C>T