Canonical Allele Identifier: CA440676044
Gene:

Linked Data

MyVariant Identifiers: chr4:g.106463824C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542667C>A , CM000666.2:g.105542667C>A GRCh38
NC_000004.11:g.106463824C>A , CM000666.1:g.106463824C>A GRCh37
NC_000004.10:g.106683273C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.338G>T
XR_939039.1:n.498G>T
XR_939040.1:n.296-1191G>T
XR_001741410.1:n.353G>T
XR_001741411.1:n.829G>T
XR_001741412.1:n.353G>T
XR_001741413.1:n.353G>T
XR_001741414.1:n.353G>T
XR_939038.2:n.353G>T
XR_939040.2:n.311-1191G>T