Canonical Allele Identifier: CA649066104

Gene:

Linked Data

• COSMIC: COSN1978027

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105542980C>A , CM000666.2:g.105542980C>A	GRCh38
NC_000004.11:g.106464137C>A , CM000666.1:g.106464137C>A	GRCh37
NC_000004.10:g.106683586C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_939038.1:n.296-271G>T
XR_939039.1:n.456-271G>T
XR_939040.1:n.296-1504G>T
XR_001741410.1:n.311-271G>T
XR_001741411.1:n.787-271G>T
XR_001741412.1:n.311-271G>T
XR_001741413.1:n.311-271G>T
XR_001741414.1:n.311-271G>T
XR_939038.2:n.311-271G>T
XR_939040.2:n.311-1504G>T