Canonical Allele Identifier: CA3153678753
Community Standard Title: NC_000007.14:g.24283850C=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24283850C= , CM000669.2:g.24283850C= GRCh38
NC_000007.13:g.24323469C= , CM000669.1:g.24323469C= GRCh37
NC_000007.12:g.24289994C= NCBI36
NG_016148.1:g.4663C=

Transcript Alleles

HGVS Amino-acid Change
XM_017012910.1:c.42-28151G= XP_016868399.1:n.42-28151G=
XM_017012911.1:c.42-28151G= XP_016868400.1:n.42-28151G=
XR_001745121.1:n.473+35507G=
XR_001745122.1:n.345-86821G=
XR_001745123.1:n.473+35507G=
XR_001745124.1:n.473+35507G=
XR_001745125.1:n.473+35507G=
XR_001745126.1:n.473+35507G=
XR_001745127.1:n.345-28151G=
XR_001745129.1:n.473+35507G=
XR_001745130.1:n.473+35507G=
XR_001745131.1:n.473+35507G=
XR_001745132.1:n.473+35507G=