Canonical Allele Identifier: CA804543381

Gene: KDM3B

Linked Data

• dbSNP Id: rs757647
• gnomAD v3: 5-138371626-G-C
• gnomAD v4: 5-138371626-G-C
• MyVariant Identifiers: chr5:g.137707315G>C (hg19) ; chr5:g.138371626G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.138371626G>C , CM000667.2:g.138371626G>C	GRCh38
NC_000005.9:g.137707315G>C , CM000667.1:g.137707315G>C	GRCh37
NC_000005.8:g.137735214G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314358.10:c.193-1048G>C MANE Select	ENSP00000326563.5:n.193-1048G>C
ENST00000314358.9:c.193-1048G>C	ENSP00000326563.5:n.193-1048G>C
NM_016604.3:c.193-1048G>C	NP_057688.2:n.193-1048G>C
XM_005272018.3:c.193-1048G>C	XP_005272075.1:n.193-1048G>C
XM_011543488.1:c.61-1048G>C	XP_011541790.1:n.61-1048G>C
XM_011543489.1:c.49-1048G>C	XP_011541791.1:n.49-1048G>C
XM_005272018.4:c.193-1048G>C	XP_005272075.1:n.193-1048G>C
XM_011543488.2:c.61-1048G>C	XP_011541790.1:n.61-1048G>C
XM_011543489.2:c.49-1048G>C	XP_011541791.1:n.49-1048G>C
XM_024446115.1:c.-282-1048G>C	XP_024301883.1:n.-282-1048G>C
NM_016604.4:c.193-1048G>C MANE Select	NP_057688.3:n.193-1048G>C