Canonical Allele Identifier: CA760353538

Gene: STK39

Linked Data

• dbSNP Id: rs1404019397
• gnomAD v3: 2-168184734-T-G
• gnomAD v4: 2-168184734-T-G
• MyVariant Identifiers: chr2:g.169041244T>G (hg19) ; chr2:g.168184734T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168184734T>G , CM000664.2:g.168184734T>G	GRCh38
NC_000002.11:g.169041244T>G , CM000664.1:g.169041244T>G	GRCh37
NC_000002.10:g.168749490T>G	NCBI36
NG_052783.1:g.67862A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697205.1:c.209-2644A>C	ENSP00000513185.1:n.209-2644A>C
ENST00000355999.5:c.209-2644A>C MANE Select	ENSP00000348278.4:n.209-2644A>C
ENST00000355999.4:c.209-2644A>C	ENSP00000348278.4:n.209-2644A>C
NM_013233.2:c.209-2644A>C	NP_037365.2:n.209-2644A>C
XM_005246465.2:c.209-2644A>C	XP_005246522.1:n.209-2644A>C
XM_011510966.1:c.209-2644A>C	XP_011509268.1:n.209-2644A>C
XM_011510967.1:c.209-2644A>C	XP_011509269.1:n.209-2644A>C
XM_011510968.1:c.209-2644A>C	XP_011509270.1:n.209-2644A>C
XM_017003813.2:c.209-2644A>C	XP_016859302.1:n.209-2644A>C
XM_017003814.2:c.209-2644A>C	XP_016859303.1:n.209-2644A>C
XM_017003815.2:c.-98-2644A>C	XP_016859304.1:n.-98-2644A>C
XM_017003816.2:c.209-2644A>C	XP_016859305.1:n.209-2644A>C
NM_013233.3:c.209-2644A>C MANE Select	NP_037365.2:n.209-2644A>C