Canonical Allele Identifier: CA440675852
Gene:

Linked Data

MyVariant Identifiers: chr4:g.106463757G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542600G>T , CM000666.2:g.105542600G>T GRCh38
NC_000004.11:g.106463757G>T , CM000666.1:g.106463757G>T GRCh37
NC_000004.10:g.106683206G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.405C>A
XR_939039.1:n.565C>A
XR_939040.1:n.296-1124C>A
XR_001741410.1:n.420C>A
XR_001741411.1:n.896C>A
XR_001741412.1:n.420C>A
XR_001741413.1:n.420C>A
XR_001741414.1:n.420C>A
XR_939038.2:n.420C>A
XR_939040.2:n.311-1124C>A