Canonical Allele Identifier: CA15909588
Gene: MYOCD HGNC NCBI

Linked Data

dbSNP Id: rs9905820
gnomAD v2: 17-12637371-T-G
gnomAD v3: 17-12734054-T-G
gnomAD v4: 17-12734054-T-G
MyVariant Identifiers: chr17:g.12637371T>G (hg19) chr17:g.12734054T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.12734054T>G , CM000679.2:g.12734054T>G GRCh38
NC_000017.10:g.12637371T>G , CM000679.1:g.12637371T>G GRCh37
NC_000017.9:g.12578096T>G NCBI36
NG_012972.1:g.73165T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000425538.6:c.416-2107T>G MANE Select ENSP00000401678.1:n.416-2107T>G
ENST00000343344.8:c.416-2107T>G ENSP00000341835.4:n.416-2107T>G
ENST00000395988.1:n.336-2107T>G
ENST00000425538.5:c.416-2107T>G ENSP00000401678.1:n.416-2107T>G
NM_001146312.2:c.416-2107T>G NP_001139784.1:n.416-2107T>G
NM_153604.3:c.416-2107T>G NP_705832.1:n.416-2107T>G
XM_005256863.1:c.416-2107T>G XP_005256920.1:n.416-2107T>G
XM_005256864.1:c.179-2107T>G XP_005256921.1:n.179-2107T>G
XM_017025342.1:c.416-2107T>G XP_016880831.1:n.416-2107T>G
NM_001146312.3:c.416-2107T>G MANE Select NP_001139784.1:n.416-2107T>G
NM_001378306.1:c.179-2107T>G NP_001365235.1:n.179-2107T>G
NM_153604.4:c.416-2107T>G NP_705832.1:n.416-2107T>G
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