Canonical Allele Identifier: CA1083366786
Gene: ADAM19 HGNC NCBI

Linked Data

dbSNP Id: rs1756964119
gnomAD v3: 5-157543196-G-A
gnomAD v4: 5-157543196-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157543196G>A , CM000667.2:g.157543196G>A GRCh38
NC_000005.9:g.156970204G>A , CM000667.1:g.156970204G>A GRCh37
NC_000005.8:g.156902782G>A NCBI36
NG_046960.1:g.37628C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000257527.9:c.252-5205C>T MANE Select ENSP00000257527.5:n.252-5205C>T
ENST00000257527.8:c.252-5205C>T ENSP00000257527.4:n.252-5205C>T
ENST00000517905.1:c.252-5205C>T ENSP00000428654.1:n.252-5205C>T
ENST00000517951.5:c.252-5205C>T ENSP00000428376.1:n.252-5205C>T
NM_033274.4:c.252-5205C>T NP_150377.1:n.252-5205C>T
XM_005266003.2:c.252-5205C>T XP_005266060.1:n.252-5205C>T
NM_033274.5:c.252-5205C>T MANE Select NP_150377.1:n.252-5205C>T
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