Canonical Allele Identifier: CA3729090

Gene: SKIC2

Linked Data

• dbSNP Id: rs756786249
• ExAC: 6:31927915 C / A
• gnomAD v2: 6-31927915-C-A
• MyVariant Identifiers: chr6:g.31927915C>A (hg19) ; chr6:g.31960138C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31960138C>A , CM000668.2:g.31960138C>A	GRCh38
NC_000006.11:g.31927915C>A , CM000668.1:g.31927915C>A	GRCh37
NC_000006.10:g.32035894C>A	NCBI36
NG_032652.1:g.6335C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461073.6:c.236+19C>A	ENSP00000419905.1:n.236+19C>A
ENST00000483553.6:c.236+19C>A	ENSP00000420332.2:n.236+19C>A
ENST00000485349.6:n.277+19C>A
ENST00000491994.2:c.236+19C>A	ENSP00000417586.2:n.236+19C>A
ENST00000494058.6:n.293+19C>A
ENST00000697831.1:c.236+19C>A	ENSP00000513453.1:n.236+19C>A
ENST00000697832.1:n.312+19C>A
ENST00000697833.1:c.236+19C>A	ENSP00000513454.1:n.236+19C>A
ENST00000697834.1:n.288+19C>A
ENST00000697835.1:c.236+19C>A	ENSP00000513455.1:n.236+19C>A
ENST00000697836.1:n.272+19C>A
ENST00000697837.1:c.236+19C>A	ENSP00000513456.1:n.236+19C>A
ENST00000697838.1:c.101+19C>A	ENSP00000513457.1:n.101+19C>A
ENST00000697839.1:n.258+19C>A
ENST00000697840.1:c.236+19C>A	ENSP00000513458.1:n.236+19C>A
ENST00000697841.1:n.247+19C>A
ENST00000697842.1:n.236+19C>A
ENST00000375394.7:c.236+19C>A MANE Select	ENSP00000364543.2:n.236+19C>A
ENST00000375394.6:c.236+19C>A	ENSP00000364543.2:n.236+19C>A
ENST00000461073.5:c.236+19C>A	ENSP00000419905.1:n.236+19C>A
ENST00000465703.5:n.288+19C>A
ENST00000474839.5:c.126+738C>A	ENSP00000420470.1:n.126+738C>A
ENST00000488648.5:n.312+19C>A
ENST00000628157.1:c.126+738C>A	ENSP00000485707.1:n.126+738C>A
NM_006929.4:c.236+19C>A	NP_008860.4:n.236+19C>A
XM_006715168.2:c.236+19C>A	XP_006715231.1:n.236+19C>A
XM_011514815.1:c.236+19C>A	XP_011513117.1:n.236+19C>A
XR_926301.1:n.324+19C>A
XM_011514815.3:c.236+19C>A	XP_011513117.1:n.236+19C>A
XR_001743586.2:n.272+19C>A
XR_926301.3:n.272+19C>A
NM_006929.5:c.236+19C>A MANE Select	NP_008860.4:n.236+19C>A