Canonical Allele Identifier: CA1083366721
Gene: ADAM19 HGNC NCBI

Linked Data

dbSNP Id: rs1756961153
gnomAD v3: 5-157543091-C-A
gnomAD v4: 5-157543091-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157543091C>A , CM000667.2:g.157543091C>A GRCh38
NC_000005.9:g.156970099C>A , CM000667.1:g.156970099C>A GRCh37
NC_000005.8:g.156902677C>A NCBI36
NG_046960.1:g.37733G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000257527.9:c.252-5100G>T MANE Select ENSP00000257527.5:n.252-5100G>T
ENST00000257527.8:c.252-5100G>T ENSP00000257527.4:n.252-5100G>T
ENST00000517905.1:c.252-5100G>T ENSP00000428654.1:n.252-5100G>T
ENST00000517951.5:c.252-5100G>T ENSP00000428376.1:n.252-5100G>T
NM_033274.4:c.252-5100G>T NP_150377.1:n.252-5100G>T
XM_005266003.2:c.252-5100G>T XP_005266060.1:n.252-5100G>T
NM_033274.5:c.252-5100G>T MANE Select NP_150377.1:n.252-5100G>T
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