Canonical Allele Identifier: CA784842279
Gene:

Linked Data

dbSNP Id: rs1335112815
gnomAD v4: 4-105542570-C-A
MyVariant Identifiers: chr4:g.106463727C>A (hg19) chr4:g.105542570C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105542570C>A , CM000666.2:g.105542570C>A GRCh38
NC_000004.11:g.106463727C>A , CM000666.1:g.106463727C>A GRCh37
NC_000004.10:g.106683176C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939038.1:n.435G>T
XR_939039.1:n.595G>T
XR_939040.1:n.296-1094G>T
XR_001741410.1:n.450G>T
XR_001741411.1:n.926G>T
XR_001741412.1:n.449+1G>T
XR_001741413.1:n.450G>T
XR_001741414.1:n.449+1G>T
XR_939038.2:n.450G>T
XR_939040.2:n.311-1094G>T
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