Canonical Allele Identifier: CA1694873321

Gene:

Linked Data

• dbSNP Id: rs17149106

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283588G>A , CM000669.2:g.24283588G>A	GRCh38
NC_000007.13:g.24323207G>A , CM000669.1:g.24323207G>A	GRCh37
NC_000007.12:g.24289732G>A	NCBI36
NG_016148.1:g.4401G>A

Transcript Alleles

HGVS	Amino-acid change
XM_017012910.1:c.42-27889C>T	XP_016868399.1:n.42-27889C>T
XM_017012911.1:c.42-27889C>T	XP_016868400.1:n.42-27889C>T
XR_001745121.1:n.473+35769C>T
XR_001745122.1:n.345-86559C>T
XR_001745123.1:n.473+35769C>T
XR_001745124.1:n.473+35769C>T
XR_001745125.1:n.473+35769C>T
XR_001745126.1:n.473+35769C>T
XR_001745127.1:n.345-27889C>T
XR_001745129.1:n.473+35769C>T
XR_001745130.1:n.473+35769C>T
XR_001745131.1:n.473+35769C>T
XR_001745132.1:n.473+35769C>T