Canonical Allele Identifier: CA103120242
Gene:

Linked Data

dbSNP Id: rs566003175
gnomAD v3: 4-102499621-G-T
gnomAD v4: 4-102499621-G-T
MyVariant Identifiers: chr4:g.103420778G>T (hg19) chr4:g.102499621G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499621G>T , CM000666.2:g.102499621G>T GRCh38
NC_000004.11:g.103420778G>T , CM000666.1:g.103420778G>T GRCh37
NC_000004.10:g.103639810G>T NCBI36
NG_050628.1:g.3293G>T

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+1628C>A XP_011530769.1:n.643+1628C>A
NR_136202.1:n.48+2818C>A
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