Canonical Allele Identifier: CA103381295

Gene:

Linked Data

• dbSNP Id: rs1053222977
• MyVariant Identifiers: chr4:g.106463792C>G (hg19) ; chr4:g.105542635C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105542635C>G , CM000666.2:g.105542635C>G	GRCh38
NC_000004.11:g.106463792C>G , CM000666.1:g.106463792C>G	GRCh37
NC_000004.10:g.106683241C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_939038.1:n.370G>C
XR_939039.1:n.530G>C
XR_939040.1:n.296-1159G>C
XR_001741410.1:n.385G>C
XR_001741411.1:n.861G>C
XR_001741412.1:n.385G>C
XR_001741413.1:n.385G>C
XR_001741414.1:n.385G>C
XR_939038.2:n.385G>C
XR_939040.2:n.311-1159G>C