Canonical Allele Identifier: CA337712305
Gene: GYG2P1 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.12272103T>C
GRCh37 chrY:g.14392807T>C
gnomAD v3:
Y:12272103 T / C
gnomAD v4:
chrY-12272103-T-C
Joint Max Group AF 0.05298804 (MID)
Genomes Max Group AF 0.04274886 (SAS)
dbSNP:
1011954
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.12272103T>C , CM000686.2:g.12272103T>C GRCh38
NC_000024.9:g.14392807T>C , CM000686.1:g.14392807T>C GRCh37
NC_000024.8:g.12902814T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651802.1:n.451-30695A>G
ENST00000651835.1:n.320-14072A>G
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