Canonical Allele Identifier: CA2408210891
Gene: SMC1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.45344156A= , CM000684.2:g.45344156A= GRCh38
NC_000022.10:g.45740037A= , CM000684.1:g.45740037A= GRCh37
NC_000022.9:g.44118701A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357450.9:c.*400T= MANE Select ENSP00000350036.4:n.*400T=
ENST00000357450.8:c.4108T= ENSP00000350036.4:n.4108T=
NM_001291501.1:c.*400T= NP_001278430.1:n.*400T=
NM_148674.4:c.*400T= NP_683515.4:n.*400T=
XM_011530144.1:c.*400T= XP_011528446.1:n.*400T=
XR_244368.3:n.4097T=
XM_011530144.2:c.*400T= XP_011528446.1:n.*400T=
XR_244368.4:n.4142T=
NM_148674.5:c.*400T= MANE Select NP_683515.4:n.*400T=
NM_001291501.2:c.*400T= NP_001278430.1:n.*400T=